Post Operative PainNCT05856682
Pre-incision Versus Lapaorscopic-assisted Transversus Abdominis Plane (TAP) and Rectus Sheath Block for Post-Cholecystectomy Pain
A study testing Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block in people with Post Operative Pain, run by Patel Hospital, Pakistan at 1 site in Pakistan.
Trial summary
The goal of this clinical trial is to compare pre-incision vs laparoscopic assisted Transversus abdominis plane and rectus sheath block in patients undergoing laparoscopic cholecystectomy. Read more about this study
- Who is it for?
- Ages 18 to 75 yearsHealthy volunteers can take part
- Conditions the study is for
- Post Operative Pain
- What is being tested?
- Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 224 participants
- Where
- 1 sitePakistan
- Study dates
- 1 Jul 2022to Aug 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 75 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Age above 18 to 75 years, both genders, Elective Laparoscopic Cholecystectomies, American Society of Anesthesiologists (ASA) physical status I \& II, Give consent.
Who cannot join
- o History of allergy , hypersentivity or contraindication to Rupivacaine, nalbuphine ,Paracetamol.
- Local skin allergy
- Laparoscopic converted to open
- Previous open upper abdominal or midline surgeries
- Diagnosis Of "Chronic Pain Syndrome"
- Known Alcohol Or Substance Abuse Within The Last 6 Months
Show all 11Show fewer
- Anti-psychotic, antidepressants, steroids use
- Multiple procedures planned under single GA
- Pregnancy
- Unable to understand i.e. deaf, language barrier, mentally incapacitated
- Coagulopathy
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Pre-incision Versus Lapaorscopic-assisted Transversus Abdominis Plane (TAP) and Rectus Sheath Block for Post-Cholecystectomy Pain Management: A Randomized Controlled Trial
The goal of this clinical trial is to compare pre-incision vs laparoscopic assisted Transversus abdominis plane and rectus sheath block in patients undergoing laparoscopic cholecystectomy. The main question it aims to answer is:
- if the effectiveness of TAP and rectus sheath block varies according to whether it is performed pre-incisional (pre emptive) or intraoperatively under Laparoscopic vision for laparoscopic cholecystectomies.
Participants will be assessed for pain at 3,6,12, and 24 hrs after surgery. Researchers will compare pain score between Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block vs Pre-incision TAP (PITAP ) .
Read the detailed description
INTRODUCTION:
Every year Over 13 million Laparoscopic procedures are performed globally. In the USA, 90% of the cholecystectomies are performed with the laparoscopic technique
- Laparoscopic cholecystectomy is the gold standard in many health centers as it is less invasive compared to open cholecystectomy.
- Good post-operative pain control, not only prevents post-operative complications but is also essential for early ambulation and return to daily routine. It is important to keep side effects minimum besides pain relieve. Therefore pre-emptive wound analgesia has been popularized. Preemptive analgesia(for eg: TAP block) is defined as an anti-nociceptive treatment that is initiated before the surgical procedure in order to reduce the sensitization (occurs because of transmission of pain signals evoked by tissue damage) of the peripheral and central pain pathways. Some analyses have shown no beneficial effect(4) whereas some have failed to reach a final conclusion regarding efficacy of pre-emptive analgesia.
- For post-laparoscopic pain management ,a multimodal approach with non-steroidal anti-inflammatory drugs, opioids and loco-regional techniques have been recommended . The Transversus Abdominis Plane (TAP) block is an analgesia technique that is loco-regional ,consists of infiltrating a local anesthetic solution between the plane of the Transversus abdominis muscle and the internal oblique muscle.
- TAP block has gradually become an alternative postoperative analgesia technology and it was described in 2001 by Rafi. . Several techniques are currently used to deliver TAP blocks, including blinded double pop technique, ultrasound-guided and laparoscopic-assisted approaches. The latter was first described in 2011 by Chetwood et al. while performing laparoscopic nephrectomies . The advantages of this technique include ease of performance, less dependency on specialized skill set or equipment, time efficient, less risk of visceral injury and avoidance of intraperitoneal local anaesthetic infiltration .
RATIONALE: Many studies have demonstrated the therapeutic benefit of laparoscopic-assisted TAP block in initial post-operative pain management in comparision with periportal local anaesthetic infiltration for patients undergoing elective laparoscopic procedures(for eg; for laparoscopic hernia repair). To the best of our knowledge, there is a paucity of data since laparoscopic-assisted TAP block has not been utilized or evaluated prospectively to see if the effectiveness of TAP block varies according to whether it is performed pre-incisional (pre emptive) or intraoperatively under Laparoscopic vision for laparoscopic cholecystectomies. Moreover, the rectus sheath block in conjunction with TAP block has not been evaluated before.
OBJECTIVE :
To compare the mean post-operative pain score at (3, 6, 12, 24 hours) with pre-incision versus laparoscopic-assisted Transversus Abdominis Plane (TAP) and Rectus sheath block in patients undergoing Laparoscopic cholecystectomy at a tertiary care hospital.
HYPOTHESIS : Post-Cholecystectomy pain control after Laparoscopic-assisted TAP block is not inferior to pain control after pre-incisional TAP block.
OPERATIONAL DEFINITIONS :
Transversus abdominis plane(TAP block): It is a regional analgesia technique which involves the injection of a local anesthetic solution into a plane between the internal oblique muscle and transversus abdominis muscle. Since the thoracolumbar nerves originating from the T6 to L1 spinal roots run into this plane and supply sensory nerves to the antero-lateral abdominal wall , the local anesthetic spread in this plane can block the neural afferents and provide analgesia to the antero-lateral abdominal wall.
Rectus sheath block : It is a method of trunk analgesia most useful for midline surgical procedures at or above the umbilicus. Local anesthetic is injected at the lateral edge of the rectus sheath where branches of the intercostal nerves enter. Instillation of local anesthetic bilaterally between the rectus muscle and the posterior sheath provides midline analgesia for several dermatomes around the injection site.
Pain score (visual analogue scale):
The Visual Analogue Scale (VAS) is the standard tool for rating of pain - either patient's own rating or rated by the health care worker. The visual analog scale is a straight line from 1 to 10 with one end meaning no pain and the other end meaning the worst pain. A patient marks a point on the line that matches the intensity of pain he or she feels.
MATERIALS AND METHODS:
- STUDY DESIGN: Double blinded, Randomized controlled trial
- SETTINGS: The study will be conducted at the department of General Surgery, Patel hospital Karachi.
- DURATION OF STUDY: After ERC approval, minimum Six months or till the sample size is achieved.
- RANDOMIZATION: Computer generated randomization table with blocks of four. Co-ordinator of HEC will have the table.
- BLINDING: Double blinded (Patient, Person assessing post-operative pain will be blinded to the both groups).
- INTERVENTION GROUP: Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block
- CONTROL GROUP: Pre-incision TAP (PITAP) block by Anesthesist.
- SAMPLE SIZE : In each arm, 112 patients.
- SAMPLE CALCULATION METHOD: Calculated using WHO software.
- Power set as =90%
- Confidence interval =95%
- Level of significance = 5%
- SAMPLING TECHNIQUE: Purposive, non probability
DATA COLLECTION PROCEDURE:
- Study will be started after approval by the institutional ethical committee.
- Detailed history, examination and relevant investigations of patients will be performed.
- Informed and written consent will be taken.
- Proforma will be filled for patients undergoing planned surgery fulfilling the inclusion criteria .
- Anesthesia will be standardized in all patients.
- All patients will receive paracetamol 1000 mg and nalbuphine 0.15mg/kg after induction of anaesthesia.
- Both the procedures will be performed by either Resident(having experience of procedure) or consultant himself/herself.
- Syringes will be prepared by one of the research team member for each patient in a designated sterile area on the day of surgery..
- Pre-incision TAP block and Rectus sheath block will be performed after induction of anesthesia, just after prep and drape by Blind double pop technique by Anesthetist/Anesthesia trainee
- Laparoscopic -assisted TAP and rectus sheath block will be performed after insertion of optical port By Surgeon /surgery trainee
- Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be Immediate right subcostal region , 3 cm medially to mid axillary line .
- The intervention and the control group will receive TAP block and rectus sheath block with Rupivacaine (3mg/kg). 1 ampule is of 10 ml and consists of 50mg /10ml, maximum dose will be 300mg. We will use a of minimum volume of solution 50ml which will be made by 3 ampules of Rupivacaine and it will be diluted to a total of 20ml of injectate( distilled water )which is then divided between the four rectus block sites (5ml each) and one TAP block site(30ml).
- Needle used for the blocks will be of 25guage and tip of the needle will be blunted by gentle tapping on metallic surface. Syringe will be of 50ml .
- Timings of PITAP AND LATAP will be noted in seconds by putting the timer on at the start of the procedures when anesthesia/surgery team calls the procedure on and by putting the timer off ,when they calls the procedure off.
- Peritoneal entry will be seen under laparoscopic vision. For LATAP ,entry would be labelled when tip of needle will be seen piercing peritoneum and for PITAP any erythema or bleed at the site of entry seen under laparoscopic vision.
- Visceral entry will be seen under laparoscopic vision for both LATAP and PITAP.
- Diet will be Regular and started after 6 hours of the surgery.
- Ambulation will be started as soon as patient is awake .
- Antibiotics (cefazolin 1gm ,q8hrly) will be prescribed post-operatively to contaminated surgery.
- Patient-controlled analgesia(PCA) will be given in the post-operative period for all patients for rescue analgesia and explained to them pre-operatively. On having pain, as per need , Patient will press the button on a pump that is connected to IV catheter. Patient will receive a preset dose of Nalbuphine 2mg.
- Pain assessment will be measured using the visual analogue scale (0-10). Pain will be assessed at both rest and coughing (reflect pain induced by physical activity) at 3,6,12, and 24 hrs after surgery by an observer blinded to both intervention and control group.
DATA ANALYSIS plan:
SPSS (ver. 16) will be used for data analysis. Confounding and effect modifying variables i.e. age, sex, diabetes are analyzed by multiple linear regression. For Data that will follow normality Independent sample T test will be applied, for data that will not follow normality Mann- whitney u test will be applied. P-value of less than 0.05 is considered statistically significant.
- Conditions
- Post Operative Pain
- Being tested
- Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block
- Medical subject headings
- Pain, Postoperative
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath blockProcedure or surgery
Also called Pre-incision TAP (PITAP) and Rectus Sheath block
Laparoscopic -assisted TAP and rectus sheath block will be performed after insertion of optical port By Surgeon /surgery trainee. • Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be anterior to the midaxillary line between the costal margin and iliac crest bilaterally.
| Study group | Role | What they receive |
|---|---|---|
| Pre-incision TAP (PITAP) and Rectus Sheath block | Active comparator | Pre-incision TAP block and Rectus sheath block will be performed after induction of anesthesia, just after prep and drape by Blind double pop technique by Anesthetist/Anesthesia trainee.Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be Immediate right subcostal region , 3 cm medially to mid axillary line The intervention and the control group will receive TAP block and rectus sheath block with Rupivacaine (3mg/kg). 1 ampule is of 10 ml and consists of 50mg /10ml, maximum dose will be 300mg. will use a of minimum volume of solution 50ml which will be made by 3 ampules of Rupivacaine and it will be diluted to a total of 20ml of injectate( distilled water )which is then divided between the four rectus block sites (5ml each) and one TAP block site(30ml ). Receives: Procedure: Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block |
| Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block | Active comparator | Laparoscopic -assisted TAP and rectus sheath block will be performed after insertion of optical port By Surgeon /surgery trainee.Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be Immediate right subcostal region , 3 cm medially to mid axillary line The intervention and the control group will receive TAP block and rectus sheath block with Rupivacaine (3mg/kg). 1 ampule is of 10 ml and consists of 50mg /10ml, maximum dose will be 300mg. will use a of minimum volume of solution 50ml which will be made by 3 ampules of Rupivacaine and it will be diluted to a total of 20ml of injectate( distilled water )which is then divided between the four rectus block sites (5ml each) and one TAP block site(30ml each). Receives: Procedure: Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block |
What is being measured
The primary outcome is the main question the study is designed to answer.
Post-operative pain changes
post operative chnage of pain score assessment at 3,6,12,24 hrs at resting and coughing. Pain score will be assessed using VAS score
Measured: 3,6,12,24 hrs post-operatively
Secondary outcomes (4)
Rescue analgesia need
if any additional anlagesia is required , nalbuphine 2mg IV as per need will be used via PCA pump.
Measured: Post operatively at 3,6,12,24hrs
Visceral Injury
if any viscera is damage during TAP and rectus sheath block in both groups
Measured: at the time of surgery
Peritoneal injury
- Peritoneal entry will be seen under laparoscopic vision. For LATAP ,entry would be labelled when tip of needle will be seen piercing peritoneum and for PITAP any erythema or bleed at the site of entry seen under laparoscopic vision.
Measured: at the time of surgery
TAP and rectus sheath block timings
comparsion of timings between both groups ,• Timings of PITAP AND LATAP will be noted in seconds by putting the timer on at the start of the procedures when anesthesia/surgery team calls the procedure on and by putting the timer off ,when they calls the procedure off.
Measured: at the time of surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 May 2023
- Study start1 Jul 2022
- Primary completionJun 2023 (estimated)
- Study completionAug 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (11)Papers the sponsor has linked to this study.
- Other trials for Post Operative PainStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- randomized, prospective, double blinded
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 224 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Patel Hospital, Pakistan
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Kanwal Nisa, Patel Hospital, Pakistan
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05856682
- Sponsor's protocol ID
- PatelHospital
- Status last verified
- May 2023
- First submitted
- 21 Apr 2023
- Last updated
- 12 May 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Amreek F, Hussain SZM, Mnagi MH, Rizwan A. Retrospective Analysis of Complications Associated with Laparoscopic Cholecystectomy for Symptomatic Gallstones. Cureus. 2019 Jul 16;11(7):e5152. doi: 10.7759/cureus.5152.
PubMed 31523579Csikesz NG, Singla A, Murphy MM, Tseng JF, Shah SA. Surgeon volume metrics in laparoscopic cholecystectomy. Dig Dis Sci. 2010 Aug;55(8):2398-405. doi: 10.1007/s10620-009-1035-6. Epub 2009 Nov 13.
PubMed 19911275Ortiz J, Rajagopalan S. A review of local anesthetic techniques for analgesia after laparoscopic surgery. J Minim Invasive Surg Sci. 2014;3:e11310
Tsai HC, Yoshida T, Chuang TY, Yang SF, Chang CC, Yao HY, Tai YT, Lin JA, Chen KY. Transversus Abdominis Plane Block: An Updated Review of Anatomy and Techniques. Biomed Res Int. 2017;2017:8284363. doi: 10.1155/2017/8284363. Epub 2017 Oct 31.
PubMed 29226150Rafi AN. Abdominal field block: a new approach via the lumbar triangle. Anaesthesia. 2001 Oct;56(10):1024-6. doi: 10.1046/j.1365-2044.2001.02279-40.x. No abstract available.
PubMed 11576144Hebbard P, Fujiwara Y, Shibata Y, Royse C. Ultrasound-guided transversus abdominis plane (TAP) block. Anaesth Intensive Care. 2007 Aug;35(4):616-7. No abstract available.
PubMed 18020088Elamin G, Waters PS, Hamid H, O'Keeffe HM, Waldron RM, Duggan M, Khan W, Barry MK, Khan IZ. Efficacy of a Laparoscopically Delivered Transversus Abdominis Plane Block Technique during Elective Laparoscopic Cholecystectomy: A Prospective, Double-Blind Randomized Trial. J Am Coll Surg. 2015 Aug;221(2):335-44. doi: 10.1016/j.jamcollsurg.2015.03.030. Epub 2015 Mar 27.
PubMed 25899736Chetwood A, Agrawal S, Hrouda D, Doyle P. Laparoscopic assisted transversus abdominis plane block: a novel insertion technique during laparoscopic nephrectomy. Anaesthesia. 2011 Apr;66(4):317-8. doi: 10.1111/j.1365-2044.2011.06664.x. No abstract available.
PubMed 21401554Mughal A, Khan A, Rehman J, Naseem H, Waldron R, Duggan M, Khan W, Barry K, Khan IZ. Laparoscopic-assisted transversus abdominis plane block as an effective analgesic in total extraperitoneal inguinal hernia repair: a double-blind, randomized controlled trial. Hernia. 2018 Oct;22(5):821-826. doi: 10.1007/s10029-018-1819-8. Epub 2018 Sep 1.
PubMed 30173291Chapter 57 - Rectus Sheath Block, Editor(s): Andrew T. Gray, Atlas of Ultrasound-Guided Regional Anesthesia (Third Edition),Elsevier, 2019,Pages 249-258,ISBN 9780323509510.
Delgado DA, Lambert BS, Boutris N, McCulloch PC, Robbins AB, Moreno MR, Harris JD. Validation of Digital Visual Analog Scale Pain Scoring With a Traditional Paper-based Visual Analog Scale in Adults. J Am Acad Orthop Surg Glob Res Rev. 2018 Mar 23;2(3):e088. doi: 10.5435/JAAOSGlobal-D-17-00088. eCollection 2018 Mar.
PubMed 30211382
Study at a glance
From the registry record, last updated by the sponsor on 12 May 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pre-incision Versus Lapaorscopic-assisted Transversus Abdominis Plane (TAP) and Rectus Sheath Block for Post-Cholecystectomy Pain Management: A Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT05856682
- Acronym / sponsor ID
- PatelHospital
- Conditions
- Post Operative Pain
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 224 participants (estimated)
- Lead sponsor
- Patel Hospital, PakistanUniversity, hospital or other
- Study start
- 1 Jul 2022 (actual)
- Primary completion
- Jun 2023 (estimated)
- Study completion
- Aug 2023 (estimated)
- First posted
- 12 May 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this clinical trial is to compare pre-incision vs laparoscopic assisted Transversus abdominis plane and rectus sheath block in patients undergoing laparoscopic cholecystectomy. The main question it aims to answer is:
- if the effectiveness of TAP and rectus sheath block varies according to whether it is performed pre-incisional (pre emptive) or intraoperatively under Laparoscopic vision for laparoscopic cholecystectomies.
Participants will be assessed for pain at 3,6,12, and 24 hrs after surgery. Researchers will compare pain score between Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block vs Pre-incision TAP (PITAP ) .
Detailed description
INTRODUCTION:
Every year Over 13 million Laparoscopic procedures are performed globally. In the USA, 90% of the cholecystectomies are performed with the laparoscopic technique
- Laparoscopic cholecystectomy is the gold standard in many health centers as it is less invasive compared to open cholecystectomy.
- Good post-operative pain control, not only prevents post-operative complications but is also essential for early ambulation and return to daily routine. It is important to keep side effects minimum besides pain relieve. Therefore pre-emptive wound analgesia has been popularized. Preemptive analgesia(for eg: TAP block) is defined as an anti-nociceptive treatment that is initiated before the surgical procedure in order to reduce the sensitization (occurs because of transmission of pain signals evoked by tissue damage) of the peripheral and central pain pathways. Some analyses have shown no beneficial effect(4) whereas some have failed to reach a final conclusion regarding efficacy of pre-emptive analgesia.
- For post-laparoscopic pain management ,a multimodal approach with non-steroidal anti-inflammatory drugs, opioids and loco-regional techniques have been recommended . The Transversus Abdominis Plane (TAP) block is an analgesia technique that is loco-regional ,consists of infiltrating a local anesthetic solution between the plane of the Transversus abdominis muscle and the internal oblique muscle.
- TAP block has gradually become an alternative postoperative analgesia technology and it was described in 2001 by Rafi. . Several techniques are currently used to deliver TAP blocks, including blinded double pop technique, ultrasound-guided and laparoscopic-assisted approaches. The latter was first described in 2011 by Chetwood et al. while performing laparoscopic nephrectomies . The advantages of this technique include ease of performance, less dependency on specialized skill set or equipment, time efficient, less risk of visceral injury and avoidance of intraperitoneal local anaesthetic infiltration .
RATIONALE: Many studies have demonstrated the therapeutic benefit of laparoscopic-assisted TAP block in initial post-operative pain management in comparision with periportal local anaesthetic infiltration for patients undergoing elective laparoscopic procedures(for eg; for laparoscopic hernia repair). To the best of our knowledge, there is a paucity of data since laparoscopic-assisted TAP block has not been utilized or evaluated prospectively to see if the effectiveness of TAP block varies according to whether it is performed pre-incisional (pre emptive) or intraoperatively under Laparoscopic vision for laparoscopic cholecystectomies. Moreover, the rectus sheath block in conjunction with TAP block has not been evaluated before.
OBJECTIVE :
To compare the mean post-operative pain score at (3, 6, 12, 24 hours) with pre-incision versus laparoscopic-assisted Transversus Abdominis Plane (TAP) and Rectus sheath block in patients undergoing Laparoscopic cholecystectomy at a tertiary care hospital.
HYPOTHESIS : Post-Cholecystectomy pain control after Laparoscopic-assisted TAP block is not inferior to pain control after pre-incisional TAP block.
OPERATIONAL DEFINITIONS :
Transversus abdominis plane(TAP block): It is a regional analgesia technique which involves the injection of a local anesthetic solution into a plane between the internal oblique muscle and transversus abdominis muscle. Since the thoracolumbar nerves originating from the T6 to L1 spinal roots run into this plane and supply sensory nerves to the antero-lateral abdominal wall , the local anesthetic spread in this plane can block the neural afferents and provide analgesia to the antero-lateral abdominal wall.
Rectus sheath block : It is a method of trunk analgesia most useful for midline surgical procedures at or above the umbilicus. Local anesthetic is injected at the lateral edge of the rectus sheath where branches of the intercostal nerves enter. Instillation of local anesthetic bilaterally between the rectus muscle and the posterior sheath provides midline analgesia for several dermatomes around the injection site.
Pain score (visual analogue scale):
The Visual Analogue Scale (VAS) is the standard tool for rating of pain - either patient's own rating or rated by the health care worker. The visual analog scale is a straight line from 1 to 10 with one end meaning no pain and the other end meaning the worst pain. A patient marks a point on the line that matches the intensity of pain he or she feels.
MATERIALS AND METHODS:
- STUDY DESIGN: Double blinded, Randomized controlled trial
- SETTINGS: The study will be conducted at the department of General Surgery, Patel hospital Karachi.
- DURATION OF STUDY: After ERC approval, minimum Six months or till the sample size is achieved.
- RANDOMIZATION: Computer generated randomization table with blocks of four. Co-ordinator of HEC will have the table.
- BLINDING: Double blinded (Patient, Person assessing post-operative pain will be blinded to the both groups).
- INTERVENTION GROUP: Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block
- CONTROL GROUP: Pre-incision TAP (PITAP) block by Anesthesist.
- SAMPLE SIZE : In each arm, 112 patients.
- SAMPLE CALCULATION METHOD: Calculated using WHO software.
- Power set as =90%
- Confidence interval =95%
- Level of significance = 5%
- SAMPLING TECHNIQUE: Purposive, non probability
DATA COLLECTION PROCEDURE:
- Study will be started after approval by the institutional ethical committee.
- Detailed history, examination and relevant investigations of patients will be performed.
- Informed and written consent will be taken.
- Proforma will be filled for patients undergoing planned surgery fulfilling the inclusion criteria .
- Anesthesia will be standardized in all patients.
- All patients will receive paracetamol 1000 mg and nalbuphine 0.15mg/kg after induction of anaesthesia.
- Both the procedures will be performed by either Resident(having experience of procedure) or consultant himself/herself.
- Syringes will be prepared by one of the research team member for each patient in a designated sterile area on the day of surgery..
- Pre-incision TAP block and Rectus sheath block will be performed after induction of anesthesia, just after prep and drape by Blind double pop technique by Anesthetist/Anesthesia trainee
- Laparoscopic -assisted TAP and rectus sheath block will be performed after insertion of optical port By Surgeon /surgery trainee
- Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be Immediate right subcostal region , 3 cm medially to mid axillary line .
- The intervention and the control group will receive TAP block and rectus sheath block with Rupivacaine (3mg/kg). 1 ampule is of 10 ml and consists of 50mg /10ml, maximum dose will be 300mg. We will use a of minimum volume of solution 50ml which will be made by 3 ampules of Rupivacaine and it will be diluted to a total of 20ml of injectate( distilled water )which is then divided between the four rectus block sites (5ml each) and one TAP block site(30ml).
- Needle used for the blocks will be of 25guage and tip of the needle will be blunted by gentle tapping on metallic surface. Syringe will be of 50ml .
- Timings of PITAP AND LATAP will be noted in seconds by putting the timer on at the start of the procedures when anesthesia/surgery team calls the procedure on and by putting the timer off ,when they calls the procedure off.
- Peritoneal entry will be seen under laparoscopic vision. For LATAP ,entry would be labelled when tip of needle will be seen piercing peritoneum and for PITAP any erythema or bleed at the site of entry seen under laparoscopic vision.
- Visceral entry will be seen under laparoscopic vision for both LATAP and PITAP.
- Diet will be Regular and started after 6 hours of the surgery.
- Ambulation will be started as soon as patient is awake .
- Antibiotics (cefazolin 1gm ,q8hrly) will be prescribed post-operatively to contaminated surgery.
- Patient-controlled analgesia(PCA) will be given in the post-operative period for all patients for rescue analgesia and explained to them pre-operatively. On having pain, as per need , Patient will press the button on a pump that is connected to IV catheter. Patient will receive a preset dose of Nalbuphine 2mg.
- Pain assessment will be measured using the visual analogue scale (0-10). Pain will be assessed at both rest and coughing (reflect pain induced by physical activity) at 3,6,12, and 24 hrs after surgery by an observer blinded to both intervention and control group.
DATA ANALYSIS plan:
SPSS (ver. 16) will be used for data analysis. Confounding and effect modifying variables i.e. age, sex, diabetes are analyzed by multiple linear regression. For Data that will follow normality Independent sample T test will be applied, for data that will not follow normality Mann- whitney u test will be applied. P-value of less than 0.05 is considered statistically significant.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
- Model description
- randomized, prospective, double blinded
| Arm | Type | Receives |
|---|---|---|
| Pre-incision TAP (PITAP) and Rectus Sheath block | Active comparator | Procedure: Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath blockPre-incision TAP block and Rectus sheath block will be performed after induction of anesthesia, just after prep and drape by Blind double pop technique by Anesthetist/Anesthesia trainee.Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be Immediate right subcostal region , 3 cm medially to mid axillary line The intervention and the control group will receive TAP block and rectus sheath block with Rupivacaine (3mg/kg). 1 ampule is of 10 ml and consists of 50mg /10ml, maximum dose will be 300mg. will use a of minimum volume of solution 50ml which will be made by 3 ampules of Rupivacaine and it will be diluted to a total of 20ml of injectate( distilled water )which is then divided between the four rectus block sites (5ml each) and one TAP block site(30ml ). |
| Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block | Active comparator | Procedure: Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath blockLaparoscopic -assisted TAP and rectus sheath block will be performed after insertion of optical port By Surgeon /surgery trainee.Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be Immediate right subcostal region , 3 cm medially to mid axillary line The intervention and the control group will receive TAP block and rectus sheath block with Rupivacaine (3mg/kg). 1 ampule is of 10 ml and consists of 50mg /10ml, maximum dose will be 300mg. will use a of minimum volume of solution 50ml which will be made by 3 ampules of Rupivacaine and it will be diluted to a total of 20ml of injectate( distilled water )which is then divided between the four rectus block sites (5ml each) and one TAP block site(30ml each). |
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Age above 18 to 75 years, both genders, Elective Laparoscopic Cholecystectomies, American Society of Anesthesiologists (ASA) physical status I \& II, Give consent.
Key exclusion criteria (11 listed)
- o History of allergy , hypersentivity or contraindication to Rupivacaine, nalbuphine ,Paracetamol.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath blockAlso: Pre-incision TAP (PITAP) and Rectus Sheath blockLaparoscopic -assisted TAP and rectus sheath block will be performed after insertion of optical port By Surgeon /surgery trainee. • Site of rectus block will be Bilaterally 3 cm lateral to Umblicus and 3cm lateral to midpoint between xiphisternum and umbilicus . Site of TAP block will be anterior to the midaxillary line between the costal margin and iliac crest bilaterally. | Procedure or surgery | Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block, Pre-incision TAP (PITAP) and Rectus Sheath block |
Primary outcome
Post-operative pain changes
Time frame: 3,6,12,24 hrs post-operatively
post operative chnage of pain score assessment at 3,6,12,24 hrs at resting and coughing. Pain score will be assessed using VAS score
4 secondary outcomes
Rescue analgesia need
Time frame: Post operatively at 3,6,12,24hrs
Visceral Injury
Time frame: at the time of surgery
Peritoneal injury
Time frame: at the time of surgery
TAP and rectus sheath block timings
Time frame: at the time of surgery
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 May 2023.
- Background: PubMed 31523579Amreek F, Hussain SZM, Mnagi MH, Rizwan A. Retrospective Analysis of Complications Associated with Laparoscopic Cholecystectomy for Symptomatic Gallstones. Cureus. 2019 Jul 16;11(7):e5152. doi: 10.7759/cureus.5152.
- Background: PubMed 19911275Csikesz NG, Singla A, Murphy MM, Tseng JF, Shah SA. Surgeon volume metrics in laparoscopic cholecystectomy. Dig Dis Sci. 2010 Aug;55(8):2398-405. doi: 10.1007/s10620-009-1035-6. Epub 2009 Nov 13.
- BackgroundOrtiz J, Rajagopalan S. A review of local anesthetic techniques for analgesia after laparoscopic surgery. J Minim Invasive Surg Sci. 2014;3:e11310
- Background: PubMed 29226150Tsai HC, Yoshida T, Chuang TY, Yang SF, Chang CC, Yao HY, Tai YT, Lin JA, Chen KY. Transversus Abdominis Plane Block: An Updated Review of Anatomy and Techniques. Biomed Res Int. 2017;2017:8284363. doi: 10.1155/2017/8284363. Epub 2017 Oct 31.
- Background: PubMed 11576144Rafi AN. Abdominal field block: a new approach via the lumbar triangle. Anaesthesia. 2001 Oct;56(10):1024-6. doi: 10.1046/j.1365-2044.2001.02279-40.x. No abstract available.
- Background: PubMed 18020088Hebbard P, Fujiwara Y, Shibata Y, Royse C. Ultrasound-guided transversus abdominis plane (TAP) block. Anaesth Intensive Care. 2007 Aug;35(4):616-7. No abstract available.
- Background: PubMed 25899736Elamin G, Waters PS, Hamid H, O'Keeffe HM, Waldron RM, Duggan M, Khan W, Barry MK, Khan IZ. Efficacy of a Laparoscopically Delivered Transversus Abdominis Plane Block Technique during Elective Laparoscopic Cholecystectomy: A Prospective, Double-Blind Randomized Trial. J Am Coll Surg. 2015 Aug;221(2):335-44. doi: 10.1016/j.jamcollsurg.2015.03.030. Epub 2015 Mar 27.
- Background: PubMed 21401554Chetwood A, Agrawal S, Hrouda D, Doyle P. Laparoscopic assisted transversus abdominis plane block: a novel insertion technique during laparoscopic nephrectomy. Anaesthesia. 2011 Apr;66(4):317-8. doi: 10.1111/j.1365-2044.2011.06664.x. No abstract available.
- Background: PubMed 30173291Mughal A, Khan A, Rehman J, Naseem H, Waldron R, Duggan M, Khan W, Barry K, Khan IZ. Laparoscopic-assisted transversus abdominis plane block as an effective analgesic in total extraperitoneal inguinal hernia repair: a double-blind, randomized controlled trial. Hernia. 2018 Oct;22(5):821-826. doi: 10.1007/s10029-018-1819-8. Epub 2018 Sep 1.
- BackgroundChapter 57 - Rectus Sheath Block, Editor(s): Andrew T. Gray, Atlas of Ultrasound-Guided Regional Anesthesia (Third Edition),Elsevier, 2019,Pages 249-258,ISBN 9780323509510.
- Background: PubMed 30211382Delgado DA, Lambert BS, Boutris N, McCulloch PC, Robbins AB, Moreno MR, Harris JD. Validation of Digital Visual Analog Scale Pain Scoring With a Traditional Paper-based Visual Analog Scale in Adults. J Am Acad Orthop Surg Glob Res Rev. 2018 Mar 23;2(3):e088. doi: 10.5435/JAAOSGlobal-D-17-00088. eCollection 2018 Mar.
- Related InfoLink provided by the sponsor.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Laparoscopic-assisted TAP block(LATAP) and Rectus Sheath block in people with Post Operative Pain, run by Patel Hospital, Pakistan at 1 site in Pakistan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 12 May 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Post-operative pain changes (time frame: 3,6,12,24 hrs post-operatively). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05856682, which also lists 11 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 May 2023.