Tonsillectomy With or Without AdenoidectomyPhase 1NCT03385057
Postoperative Ibuprofen Use and Risk of Bleeding in Pediatric Tonsillectomy
A Phase 1 study testing Ibuprofen and Acetaminophen in people with Tonsillectomy With or Without Adenoidectomy, run by Massachusetts Eye and Ear Infirmary at 5 sites in United States.
Trial summary
Pediatric tonsillectomy is one of the most common surgical procedures annually in the United States; risks include postoperative hemorrhage and poor pain control. Controversy exists regarding optimal pharmacologic pain management following surgery, as each drug's efficacy is balanced by its specific side effects. Read more about this study
- Who is it for?
- Ages 2 to 18 years
- Conditions the study is for
- Tonsillectomy With or Without Adenoidectomy
- What is being tested?
- Ibuprofen and Acetaminophen
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 0 participants
- Where
- 5 sitesUnited States
- Study dates
- Sep 2018to 1 Jan 2023
- Phase
- Phase 1
- 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 2 to 18 years
- All sexes
- No healthy volunteers
- Child, Adult
Who may be able to join
- Male and female patients ages 2-18 undergoing tonsillectomy with or without adenoidectomy by electrocautery alone for all indications
- Patients with complex medical conditions and craniofacial abnormalities will be included.
- Family must understand and be able to read English.
- Only patients who are not pregnant will be included.
- Informed consent and, child assent (when appropriate) will be required for enrollment. Patients will provide signed and dated informed consent form.
- Subjects will be willing and able to comply with all study procedures and be available for the duration of the study.
Who cannot join
- Patients with a known personal or family history of a bleeding disorder.
- Patients with a history of asthma, kidney or liver problems.
- Patients with tonsillectomy or adenoidectomy performed using a cold knife technique, microdebrider, coblation or plasma knife.
- Patients on NSAIDs for other medical conditions or those who have taken NSAIDs within 1 week of surgery
- Patients with allergy to aspirin or other NSAIDs, acetaminophen, Red Dye #40 or Red Dye #33
- Patients found to be pregnant will be excluded from participation. Pregnancy testing using urine beta-HCG will be performed on all children > 13 years of age, or those younger than 13 who are menstruating; this is the testing protocol used at the Children's Hospital of Boston.
- Patients unwilling to enroll in the study will have the tonsillectomy with or without adenoidectomy performed according to current practice standards.
Trial locations and contacts
5 sites in 1 country.
5 sites in 1 country
United States5 sites
Emory University and Children's Healthcare of Atlanta
Atlanta, Georgia, 30322
Case Western University- Raimbow Babies and Children's
Cleveland, Ohio, 44106
Portsmouth Naval Hospital
Portsmouth, Virginia, 23708-2197
Rady's Children's Hospital
San Diego, California, 92123
Madigan Army Hospital
Tacoma, Washington, 98431
About this study
Pediatric tonsillectomy is one of the most common surgical procedures annually in the United States; risks include postoperative hemorrhage and poor pain control. Controversy exists regarding optimal pharmacologic pain management following surgery, as each drug's efficacy is balanced by its specific side effects. Ibuprofen is effective in controlling postoperative pain following tonsillectomy, but its mechanism of action results in decreased platelet function, which may increase postoperative bleeding events. This is a multicenter, randomized control non-inferiority trial designed to assess the relationship between short-course ibuprofen use and post-tonsillectomy bleeding when compared to acetaminophen.
Read the detailed description
Pediatric tonsillectomy is one of the most common surgical procedures in the United States, with over 500,000 procedures performed annually.1,2 The most common indications for tonsillectomy with and without adenoidectomy are sleep-disordered breathing and recurrent tonsillitis, though significant demographic and regional variation exist.2 In recent years, particular attention has been paid to the deleterious sequelae of pediatric obstructive sleep apnea on children's behavior, cognition, and growth as well as its negative effects on long-term pulmonary and cardiovascular health.3-5 Tonsillectomy is generally considered a safe procedure, though potential exists for significant procedural morbidity. Potential risks associated with tonsillectomy include postoperative hemorrhage, airway risk, aspiration, burn injury, post-operative nausea and vomiting, and poor pain control.6,7 Postoperative hemorrhage is the most serious post-tonsillectomy complication and can be divided according to timing (primary occurring <24 hours from surgery, or secondary occurring >24 hours after surgery) and severity (level 1: any history of bleeding, level 2: bleeding requiring inpatient admission, level 3: bleeding requiring operative intervention). Following discharge, inadequate analgesia can result in secondary complications such as dehydration, nausea, bleeding, hospital readmission, and increased healthcare expenditures.8,9
Significant controversy exists as to the optimal pain management protocol following pediatric tonsillectomy.8,9 Many studies have examined both pharmacologic and non-pharmacologic modalities to improve pain control in this population. The most common medications prescribed after tonsillectomy include acetaminophen (paracetamol), non-steroidal anti-inflammatory drugs (NSAIDs) (e.g. ibuprofen), and narcotic pain medications, each with a unique mode of action and risk profile.8,10-12 Acetaminophen, which has both peripheral and central anti-nociceptive properties, is generally well-tolerated with low incidence of serious side effects, but may not provide adequate pain control when used at recommended pediatric dosages.13 Narcotic (opioid) pain medications act on the mu opioid receptor and effectively decrease sensory and affective components of pain.14 Unfortunately, opioid pain medications also result in dose-dependent respiratory depression; a significant contraindication in patients with sleep-disordered breathing.15,16 The FDA has released a warning cautioning against the use of codeine, an opioid, for postoperative analgesia following tonsillectomy.7 Furthermore, emerging data suggests that adolescent patients receiving prescription for narcotic pain medication may be at risk for long-term opioid dependence and addiction.17 NSAIDs provide analgesia through reversible COX-1 and COX-2 pathway inhibition which results in decreased prostaglandin-induced inflammation and edema.18 This mechanism of action also interferes with platelet aggregation, potentially impacting bleeding in the postoperative period. Ibuprofen, a derivative of propionic acid, is one of the most commonly prescribed NSAID medications, with a half-life of less than 12 hours.19,20 Pain control in patients receiving NSAIDs is equivalent, or superior to, those receiving acetaminophen alone or in combination with narcotic medication.21-23 In 2011, the American Academy of Pediatrics released its Clinical Practice Guidelines, which stated that ibuprofen can safely be used for postoperative analgesia following tonsillectomy24, a recommendation based on a 2005 Cochrane Review of NSAIDs and post-tonsillectomy bleeding. The most recent Cochrane review on this topic, published in 2012 and based on 15 randomized control trials (RCTs), concludes that there is insufficient evidence available to exclude an increased risk of bleeding with NSAID use following pediatric tonsillectomy.25 This is supported by data from a prospective, randomized control non-inferiority trial conducted at our own institution, in which participants received either ibuprofen or acetaminophen for 9 days following surgery. In this study, an increased rate of post-tonsillectomy bleeding requiring operative intervention could not be excluded because the non-inferiority threshold was crossed. The duration of safe NSAID use, if any, after tonsillectomy is unknown. A study definitively documenting safety and efficacy of short-course NSAID administration following tonsillectomy in children would affect our own standard of care as well as overall clinical practice guidelines.
This study serves as a follow-up clinical trial to a double-blind randomized control non-inferiority trial titled "Postoperative Ibuprofen and the Risk of Bleeding After Tonsillectomy with or without Adenoidectomy" conducted from 2012 to 2016 at Massachusetts Eye and Ear and collaborating institutions. In this study, participants were randomized to receive either ibuprofen (10 mg/kg every 6 hours) or acetaminophen (15 mg/kg every 6 hours) for 9 days following surgery. The non-inferiority margin was set at 3%. Increased type 3 bleeding (bleeding requiring operative intervention) could not be excluded because the non-inferiority threshold was crossed.
In this study, type 3 bleeding occurred in the ibuprofen group on an average postoperative day of 5.95. Additional analyses were conducted on study subjects who discontinued the study drugs prior to postoperative day 9 (the scheduled end point). A total of 50 patients discontinued study medication on or before postoperative day 3. Of these, 21 were randomized to the ibuprofen arm and 0/21 experienced postoperative bleeding events.
A recent systematic review by Tan et al examined commonly used medications following tonsillectomy and efficacy and risks associated with each drug.8 Acetaminophen is commonly used following tonsillectomy given its low side effect profile; however, analgesia is often inadequate at recommended dosages.26 Despite a 2013 FDA warning cautioning against opioid use following pediatric tonsillectomy due to increased risk of respiratory depression, these medications continue to be prescribed following surgery. The majority of tonsillectomies are now performed for sleep apnea and sleep disordered breathing; therefore, a large proportion of patients have increased risk of respiratory compromise and desaturations following surgery when opioid medications are administered.22 Furthermore, emerging data suggests that a significant fraction of adolescent patients receiving opioid pain medications postoperatively may subsequently develop addiction to these medications.17 NSAIDs are effective for post-tonsillectomy analgesia, but concerns remain regarding increased risk of postoperative hemorrhage with use of these medications despite current American Academy of Pediatrics recommendations advocate that ibuprofen may be safely utilized following tonsillectomy in children. Studies to date demonstrate conflicting or equivocal results with regard to increased bleeding risk following NSAID administration. Given previous data from this institution which cannot exclude increased incidence of type 3 bleeding following 9 days of ibuprofen exposure, MEE standard of practice is to recommend against extended duration of ibuprofen use in the postoplerative period. However, given concerns of inadequate analgesia with acetaminophen and respiratory depression and addictive potential with opioid medication, we feel that it is important to assess for postoperative time interval where NSAID medications may be safely administered without increasing incidence of postoperative bleeding events.
We propose a study comparing impact of maximally-dosed ibuprofen (10 mg/kg every 6 hours) versus maximally-dosed acetaminophen (15 mg/kg every 6 hours) on postoperative pain and bleeding when administered for four days (short-course) to children age 2-18 undergoing tonsillectomy with or without adenoidectomy. We believe that a four-day course of medication is appropriate given that the majority of post-tonsillectomy bleeding events occurred on day 6 and the half-life of ibuprofen is such that platelet function returns to baseline within 24 hours of drug discontinuation20. We hypothesize that children aged 2-18 receiving short-course ibuprofen following tonsillectomy will not have increased incidence of bleeding when compared to patients receiving acetaminophen postoperatively. A study definitively documenting safety and efficacy of short-course NSAID administration following tonsillectomy in children would affect our own standard of care as well as overall clinical practice guidelines surrounding this procedure.
- Being tested
- Ibuprofen, Acetaminophen
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
IbuprofenDrug
Also called Motrin
Grape-flavored ibuprofen 100mg/5mL (Leader®) will be dispensed. Ibuprofen will be dosed at 10mg/kg (max dose 600mg) QID (roughly Q6 hours, however we left dosing QID to allow for some flexibility in the dosing schedule to accommodate patient sleeping schedules). The pharmacy will manipulate the volume of each medication using Ora Blend suspension so that for each child, weight-based dosing of each medication will be equivalent in volume. The first dose of study medication will be dispensed 4 hours after the preoperative acetaminophen dose. Thereafter, medication will be dosed QID (or roughly 6 hours apart). Surgeons, nursing staff, and patients and their families will be blinded regarding the type of medication administered.
AcetaminophenDrug
Also called Advil
Grape-flavored acetaminophen 160mg/5mL (Leader®) will be dispensed based upon the arm to which each participant has been randomized. Acetaminophen at 15mg/kg (max dose 650mg), dosing will be QID (roughly Q6 hours, however we left dosing QID to allow for some flexibility in the dosing schedule to accommodate patient sleeping schedules). The pharmacy will manipulate the volume of each medication using Ora Blend suspension so that for each child, weight-based dosing of each medication will be equivalent in volume. The first dose of study medication will be dispensed 4 hours after the preoperative acetaminophen dose. Thereafter, medication will be dosed QID (or roughly 6 hours apart). Surgeons, nursing staff, and patients and their families will be blinded regarding the type of medication administered.
| Study group | Role | What they receive |
|---|---|---|
| Ibuprofen Arm | Active comparator | Not described Receives: Drug: Ibuprofen |
| Acetaminophen | Active comparator | Not described Receives: Drug: Acetaminophen |
What is being measured
The primary outcome is the main question the study is designed to answer.
Post-tonsillectomy bleeding within 14 days of surgery.
This will be classified by timing (<24 hours vs. 24 hours or more) and severity (level 1: bleeding by history alone; level 2: objective bleeding requiring hospital admission and observation; level 3: objective bleeding requiring operative intervention). Bleeding events will be documented during postoperative visit at two weeks as well as through medical record review.
Measured: Within 14 days of surgery
Secondary outcomes (1)
Post-tonsillectomy pain control data through 14 days of surgery
Post-tonsillectomy pain control data through 14 days of surgery. Patients and family members will receive validated pain control questionnaires to be filled out every day for the first 14 days following surgery (see Appendix ).
Measured: Through 14 days of surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Dec 2017
- Study startSep 2018 (estimated)
- Primary completion1 Jan 2023 (estimated)
- Study completion1 Jan 2023 (estimated)
Why it stopped: Study design flaws; research design needed to be reconfigured
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (23)Papers the sponsor has linked to this study.
- Other trials for Tonsillectomy With or Without AdenoidectomyStudies 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 1
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Participant, Care provider, Investigator
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- Massachusetts Eye and Ear Infirmary
- Sponsor type
- University, hospital or other
- Collaborators
- Emory University, University Hospitals Cleveland Medical Center, Madigan Army Medical Center, United States Naval Medical Center, Portsmouth, Rady Children's Hospital, San Diego
- Responsible party
- Sponsor
- Investigators
- Christopher J Hartnick, MD, Principal investigator, Massachusetts Eye and Ear
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03385057
- Sponsor's protocol ID
- 17-167H
- Status last verified
- Sep 2018
- First submitted
- 20 Dec 2017
- Last updated
- 20 Sep 2018
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Baugh RF, Archer SM, Mitchell RB, Rosenfeld RM, Amin R, Burns JJ, Darrow DH, Giordano T, Litman RS, Li KK, Mannix ME, Schwartz RH, Setzen G, Wald ER, Wall E, Sandberg G, Patel MM; American Academy of Otolaryngology-Head and Neck Surgery Foundation. Clinical practice guideline: tonsillectomy in children. Otolaryngol Head Neck Surg. 2011 Jan;144(1 Suppl):S1-30. doi: 10.1177/0194599810389949.
PubMed 21493257Boss EF, Marsteller JA, Simon AE. Outpatient tonsillectomy in children: demographic and geographic variation in the United States, 2006. J Pediatr. 2012 May;160(5):814-9. doi: 10.1016/j.jpeds.2011.11.041. Epub 2011 Dec 17.
PubMed 22183449Alexander NS, Schroeder JW Jr. Pediatric obstructive sleep apnea syndrome. Pediatr Clin North Am. 2013 Aug;60(4):827-40. doi: 10.1016/j.pcl.2013.04.009.
PubMed 23905822Schwengel DA, Dalesio NM, Stierer TL. Pediatric obstructive sleep apnea. Anesthesiol Clin. 2014 Mar;32(1):237-61. doi: 10.1016/j.anclin.2013.10.012.
PubMed 24491659Spicuzza L, Leonardi S, La Rosa M. Pediatric sleep apnea: early onset of the 'syndrome'? Sleep Med Rev. 2009 Apr;13(2):111-22. doi: 10.1016/j.smrv.2008.07.001. Epub 2008 Dec 5.
PubMed 19058983Randall DA, Hoffer ME. Complications of tonsillectomy and adenoidectomy. Otolaryngol Head Neck Surg. 1998 Jan;118(1):61-8. doi: 10.1016/S0194-5998(98)70376-6.
PubMed 9450830Subramanyam R, Varughese A, Willging JP, Sadhasivam S. Future of pediatric tonsillectomy and perioperative outcomes. Int J Pediatr Otorhinolaryngol. 2013 Feb;77(2):194-9. doi: 10.1016/j.ijporl.2012.10.016. Epub 2012 Nov 16.
PubMed 23159321Tan GX, Tunkel DE. Control of Pain After Tonsillectomy in Children: A Review. JAMA Otolaryngol Head Neck Surg. 2017 Sep 1;143(9):937-942. doi: 10.1001/jamaoto.2017.0845.
PubMed 28662233Cohen N, Sommer DD. Post-tonsillectomy pain control: consensus or controversy? Pain Manag. 2016;6(1):31-7. doi: 10.2217/pmt.15.58. Epub 2015 Dec 17.
PubMed 26678541Moir MS, Bair E, Shinnick P, Messner A. Acetaminophen versus acetaminophen with codeine after pediatric tonsillectomy. Laryngoscope. 2000 Nov;110(11):1824-7. doi: 10.1097/00005537-200011000-00011.
PubMed 11081593Isaacson G. Pediatric tonsillectomy: an evidence-based approach. Otolaryngol Clin North Am. 2014 Oct;47(5):673-90. doi: 10.1016/j.otc.2014.06.011. Epub 2014 Aug 7.
PubMed 25213277Isaacson G. Tonsillectomy care for the pediatrician. Pediatrics. 2012 Aug;130(2):324-34. doi: 10.1542/peds.2011-3857. Epub 2012 Jul 2.
PubMed 22753552Romsing J, Hertel S, Harder A, Rasmussen M. Examination of acetaminophen for outpatient management of postoperative pain in children. Paediatr Anaesth. 1998;8(3):235-9. doi: 10.1046/j.1460-9592.1998.00768.x.
PubMed 9608969Zubieta JK, Smith YR, Bueller JA, Xu Y, Kilbourn MR, Jewett DM, Meyer CR, Koeppe RA, Stohler CS. Regional mu opioid receptor regulation of sensory and affective dimensions of pain. Science. 2001 Jul 13;293(5528):311-5. doi: 10.1126/science.1060952.
PubMed 11452128Sadhasivam S, Myer CM 3rd. Preventing opioid-related deaths in children undergoing surgery. Pain Med. 2012 Jul;13(7):982-3; author reply 984. doi: 10.1111/j.1526-4637.2012.01419.x. Epub 2012 Jun 13.
PubMed 22694279
Study at a glance
From the registry record, last updated by the sponsor on 20 Sep 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Postoperative Ibuprofen Use and Risk of Bleeding in Pediatric Tonsillectomy
- ClinicalTrials.gov ID
- NCT03385057
- Acronym / sponsor ID
- 17-167H
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- WithdrawnReason stopped: Study design flaws; research design needed to be reconfigured
- Enrolment
- 0 participants (actual)
- Lead sponsor
- Massachusetts Eye and Ear InfirmaryUniversity, hospital or other
- Collaborators
- Emory University, University Hospitals Cleveland Medical Center, Madigan Army Medical Center, United States Naval Medical Center, Portsmouth, Rady Children's Hospital, San Diego
- Study start
- Sep 2018 (estimated)
- Primary completion
- 1 Jan 2023 (estimated)
- Study completion
- 1 Jan 2023 (estimated)
- First posted
- 28 Dec 2017 (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.
Pediatric tonsillectomy is one of the most common surgical procedures annually in the United States; risks include postoperative hemorrhage and poor pain control. Controversy exists regarding optimal pharmacologic pain management following surgery, as each drug's efficacy is balanced by its specific side effects. Ibuprofen is effective in controlling postoperative pain following tonsillectomy, but its mechanism of action results in decreased platelet function, which may increase postoperative bleeding events. This is a multicenter, randomized control non-inferiority trial designed to assess the relationship between short-course ibuprofen use and post-tonsillectomy bleeding when compared to acetaminophen.
Detailed description
Pediatric tonsillectomy is one of the most common surgical procedures in the United States, with over 500,000 procedures performed annually.1,2 The most common indications for tonsillectomy with and without adenoidectomy are sleep-disordered breathing and recurrent tonsillitis, though significant demographic and regional variation exist.2 In recent years, particular attention has been paid to the deleterious sequelae of pediatric obstructive sleep apnea on children's behavior, cognition, and growth as well as its negative effects on long-term pulmonary and cardiovascular health.3-5 Tonsillectomy is generally considered a safe procedure, though potential exists for significant procedural morbidity. Potential risks associated with tonsillectomy include postoperative hemorrhage, airway risk, aspiration, burn injury, post-operative nausea and vomiting, and poor pain control.6,7 Postoperative hemorrhage is the most serious post-tonsillectomy complication and can be divided according to timing (primary occurring <24 hours from surgery, or secondary occurring >24 hours after surgery) and severity (level 1: any history of bleeding, level 2: bleeding requiring inpatient admission, level 3: bleeding requiring operative intervention). Following discharge, inadequate analgesia can result in secondary complications such as dehydration, nausea, bleeding, hospital readmission, and increased healthcare expenditures.8,9
Significant controversy exists as to the optimal pain management protocol following pediatric tonsillectomy.8,9 Many studies have examined both pharmacologic and non-pharmacologic modalities to improve pain control in this population. The most common medications prescribed after tonsillectomy include acetaminophen (paracetamol), non-steroidal anti-inflammatory drugs (NSAIDs) (e.g. ibuprofen), and narcotic pain medications, each with a unique mode of action and risk profile.8,10-12 Acetaminophen, which has both peripheral and central anti-nociceptive properties, is generally well-tolerated with low incidence of serious side effects, but may not provide adequate pain control when used at recommended pediatric dosages.13 Narcotic (opioid) pain medications act on the mu opioid receptor and effectively decrease sensory and affective components of pain.14 Unfortunately, opioid pain medications also result in dose-dependent respiratory depression; a significant contraindication in patients with sleep-disordered breathing.15,16 The FDA has released a warning cautioning against the use of codeine, an opioid, for postoperative analgesia following tonsillectomy.7 Furthermore, emerging data suggests that adolescent patients receiving prescription for narcotic pain medication may be at risk for long-term opioid dependence and addiction.17 NSAIDs provide analgesia through reversible COX-1 and COX-2 pathway inhibition which results in decreased prostaglandin-induced inflammation and edema.18 This mechanism of action also interferes with platelet aggregation, potentially impacting bleeding in the postoperative period. Ibuprofen, a derivative of propionic acid, is one of the most commonly prescribed NSAID medications, with a half-life of less than 12 hours.19,20 Pain control in patients receiving NSAIDs is equivalent, or superior to, those receiving acetaminophen alone or in combination with narcotic medication.21-23 In 2011, the American Academy of Pediatrics released its Clinical Practice Guidelines, which stated that ibuprofen can safely be used for postoperative analgesia following tonsillectomy24, a recommendation based on a 2005 Cochrane Review of NSAIDs and post-tonsillectomy bleeding. The most recent Cochrane review on this topic, published in 2012 and based on 15 randomized control trials (RCTs), concludes that there is insufficient evidence available to exclude an increased risk of bleeding with NSAID use following pediatric tonsillectomy.25 This is supported by data from a prospective, randomized control non-inferiority trial conducted at our own institution, in which participants received either ibuprofen or acetaminophen for 9 days following surgery. In this study, an increased rate of post-tonsillectomy bleeding requiring operative intervention could not be excluded because the non-inferiority threshold was crossed. The duration of safe NSAID use, if any, after tonsillectomy is unknown. A study definitively documenting safety and efficacy of short-course NSAID administration following tonsillectomy in children would affect our own standard of care as well as overall clinical practice guidelines.
This study serves as a follow-up clinical trial to a double-blind randomized control non-inferiority trial titled "Postoperative Ibuprofen and the Risk of Bleeding After Tonsillectomy with or without Adenoidectomy" conducted from 2012 to 2016 at Massachusetts Eye and Ear and collaborating institutions. In this study, participants were randomized to receive either ibuprofen (10 mg/kg every 6 hours) or acetaminophen (15 mg/kg every 6 hours) for 9 days following surgery. The non-inferiority margin was set at 3%. Increased type 3 bleeding (bleeding requiring operative intervention) could not be excluded because the non-inferiority threshold was crossed.
In this study, type 3 bleeding occurred in the ibuprofen group on an average postoperative day of 5.95. Additional analyses were conducted on study subjects who discontinued the study drugs prior to postoperative day 9 (the scheduled end point). A total of 50 patients discontinued study medication on or before postoperative day 3. Of these, 21 were randomized to the ibuprofen arm and 0/21 experienced postoperative bleeding events.
A recent systematic review by Tan et al examined commonly used medications following tonsillectomy and efficacy and risks associated with each drug.8 Acetaminophen is commonly used following tonsillectomy given its low side effect profile; however, analgesia is often inadequate at recommended dosages.26 Despite a 2013 FDA warning cautioning against opioid use following pediatric tonsillectomy due to increased risk of respiratory depression, these medications continue to be prescribed following surgery. The majority of tonsillectomies are now performed for sleep apnea and sleep disordered breathing; therefore, a large proportion of patients have increased risk of respiratory compromise and desaturations following surgery when opioid medications are administered.22 Furthermore, emerging data suggests that a significant fraction of adolescent patients receiving opioid pain medications postoperatively may subsequently develop addiction to these medications.17 NSAIDs are effective for post-tonsillectomy analgesia, but concerns remain regarding increased risk of postoperative hemorrhage with use of these medications despite current American Academy of Pediatrics recommendations advocate that ibuprofen may be safely utilized following tonsillectomy in children. Studies to date demonstrate conflicting or equivocal results with regard to increased bleeding risk following NSAID administration. Given previous data from this institution which cannot exclude increased incidence of type 3 bleeding following 9 days of ibuprofen exposure, MEE standard of practice is to recommend against extended duration of ibuprofen use in the postoplerative period. However, given concerns of inadequate analgesia with acetaminophen and respiratory depression and addictive potential with opioid medication, we feel that it is important to assess for postoperative time interval where NSAID medications may be safely administered without increasing incidence of postoperative bleeding events.
We propose a study comparing impact of maximally-dosed ibuprofen (10 mg/kg every 6 hours) versus maximally-dosed acetaminophen (15 mg/kg every 6 hours) on postoperative pain and bleeding when administered for four days (short-course) to children age 2-18 undergoing tonsillectomy with or without adenoidectomy. We believe that a four-day course of medication is appropriate given that the majority of post-tonsillectomy bleeding events occurred on day 6 and the half-life of ibuprofen is such that platelet function returns to baseline within 24 hours of drug discontinuation20. We hypothesize that children aged 2-18 receiving short-course ibuprofen following tonsillectomy will not have increased incidence of bleeding when compared to patients receiving acetaminophen postoperatively. A study definitively documenting safety and efficacy of short-course NSAID administration following tonsillectomy in children would affect our own standard of care as well as overall clinical practice guidelines surrounding this procedure.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, care provider, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Ibuprofen Arm | Active comparator | Drug: Ibuprofen |
| Acetaminophen | Active comparator | Drug: Acetaminophen |
Who may qualify
- Ages
- 2 to 18 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Key inclusion criteria (6 listed)
- Male and female patients ages 2-18 undergoing tonsillectomy with or without adenoidectomy by electrocautery alone for all indications
- Patients with complex medical conditions and craniofacial abnormalities will be included.
- Family must understand and be able to read English.
- Only patients who are not pregnant will be included.
- Informed consent and, child assent (when appropriate) will be required for enrollment. Patients will provide signed and dated informed consent form.
Key exclusion criteria (7 listed)
- Patients with a known personal or family history of a bleeding disorder.
- Patients with a history of asthma, kidney or liver problems.
- Patients with tonsillectomy or adenoidectomy performed using a cold knife technique, microdebrider, coblation or plasma knife.
- Patients on NSAIDs for other medical conditions or those who have taken NSAIDs within 1 week of surgery
- Patients with allergy to aspirin or other NSAIDs, acetaminophen, Red Dye #40 or Red Dye #33
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 |
|---|---|---|
| IbuprofenAlso: MotrinGrape-flavored ibuprofen 100mg/5mL (Leader®) will be dispensed. Ibuprofen will be dosed at 10mg/kg (max dose 600mg) QID (roughly Q6 hours, however we left dosing QID to allow for some flexibility in the dosing schedule to accommodate patient sleeping schedules). The pharmacy will manipulate the volume of each medication using Ora Blend suspension so that for each child, weight-based dosing of each medication will be equivalent in volume. The first dose of study medication will be dispensed 4 hours after the preoperative acetaminophen dose. Thereafter, medication will be dosed QID (or roughly 6 hours apart). Surgeons, nursing staff, and patients and their families will be blinded regarding the type of medication administered. | Drug | Ibuprofen Arm |
| AcetaminophenAlso: AdvilGrape-flavored acetaminophen 160mg/5mL (Leader®) will be dispensed based upon the arm to which each participant has been randomized. Acetaminophen at 15mg/kg (max dose 650mg), dosing will be QID (roughly Q6 hours, however we left dosing QID to allow for some flexibility in the dosing schedule to accommodate patient sleeping schedules). The pharmacy will manipulate the volume of each medication using Ora Blend suspension so that for each child, weight-based dosing of each medication will be equivalent in volume. The first dose of study medication will be dispensed 4 hours after the preoperative acetaminophen dose. Thereafter, medication will be dosed QID (or roughly 6 hours apart). Surgeons, nursing staff, and patients and their families will be blinded regarding the type of medication administered. | Drug | Acetaminophen |
Primary outcome
Post-tonsillectomy bleeding within 14 days of surgery.
Time frame: Within 14 days of surgery
This will be classified by timing (<24 hours vs. 24 hours or more) and severity (level 1: bleeding by history alone; level 2: objective bleeding requiring hospital admission and observation; level 3: objective bleeding requiring operative intervention). Bleeding events will be documented during postoperative visit at two weeks as well as through medical record review.
1 secondary outcome
Post-tonsillectomy pain control data through 14 days of surgery
Time frame: Through 14 days of surgery
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Sep 2018.
- Background: PubMed 21493257Baugh RF, Archer SM, Mitchell RB, Rosenfeld RM, Amin R, Burns JJ, Darrow DH, Giordano T, Litman RS, Li KK, Mannix ME, Schwartz RH, Setzen G, Wald ER, Wall E, Sandberg G, Patel MM; American Academy of Otolaryngology-Head and Neck Surgery Foundation. Clinical practice guideline: tonsillectomy in children. Otolaryngol Head Neck Surg. 2011 Jan;144(1 Suppl):S1-30. doi: 10.1177/0194599810389949.
- Background: PubMed 22183449Boss EF, Marsteller JA, Simon AE. Outpatient tonsillectomy in children: demographic and geographic variation in the United States, 2006. J Pediatr. 2012 May;160(5):814-9. doi: 10.1016/j.jpeds.2011.11.041. Epub 2011 Dec 17.
- Background: PubMed 23905822Alexander NS, Schroeder JW Jr. Pediatric obstructive sleep apnea syndrome. Pediatr Clin North Am. 2013 Aug;60(4):827-40. doi: 10.1016/j.pcl.2013.04.009.
- Background: PubMed 24491659Schwengel DA, Dalesio NM, Stierer TL. Pediatric obstructive sleep apnea. Anesthesiol Clin. 2014 Mar;32(1):237-61. doi: 10.1016/j.anclin.2013.10.012.
- Background: PubMed 19058983Spicuzza L, Leonardi S, La Rosa M. Pediatric sleep apnea: early onset of the 'syndrome'? Sleep Med Rev. 2009 Apr;13(2):111-22. doi: 10.1016/j.smrv.2008.07.001. Epub 2008 Dec 5.
- Background: PubMed 9450830Randall DA, Hoffer ME. Complications of tonsillectomy and adenoidectomy. Otolaryngol Head Neck Surg. 1998 Jan;118(1):61-8. doi: 10.1016/S0194-5998(98)70376-6.
- Background: PubMed 23159321Subramanyam R, Varughese A, Willging JP, Sadhasivam S. Future of pediatric tonsillectomy and perioperative outcomes. Int J Pediatr Otorhinolaryngol. 2013 Feb;77(2):194-9. doi: 10.1016/j.ijporl.2012.10.016. Epub 2012 Nov 16.
- Background: PubMed 28662233Tan GX, Tunkel DE. Control of Pain After Tonsillectomy in Children: A Review. JAMA Otolaryngol Head Neck Surg. 2017 Sep 1;143(9):937-942. doi: 10.1001/jamaoto.2017.0845.
- Background: PubMed 26678541Cohen N, Sommer DD. Post-tonsillectomy pain control: consensus or controversy? Pain Manag. 2016;6(1):31-7. doi: 10.2217/pmt.15.58. Epub 2015 Dec 17.
- Background: PubMed 11081593Moir MS, Bair E, Shinnick P, Messner A. Acetaminophen versus acetaminophen with codeine after pediatric tonsillectomy. Laryngoscope. 2000 Nov;110(11):1824-7. doi: 10.1097/00005537-200011000-00011.
- Background: PubMed 25213277Isaacson G. Pediatric tonsillectomy: an evidence-based approach. Otolaryngol Clin North Am. 2014 Oct;47(5):673-90. doi: 10.1016/j.otc.2014.06.011. Epub 2014 Aug 7.
- Background: PubMed 22753552Isaacson G. Tonsillectomy care for the pediatrician. Pediatrics. 2012 Aug;130(2):324-34. doi: 10.1542/peds.2011-3857. Epub 2012 Jul 2.
- Individual participant dataSharing planned: Undecided
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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.
Christopher J Hartnick, MD principal investigator
Massachusetts Eye and Ear
5 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing Ibuprofen and Acetaminophen in people with Tonsillectomy With or Without Adenoidectomy, run by Massachusetts Eye and Ear Infirmary at 5 sites in United States.
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 6 inclusion and 7 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: withdrawn, as of the sponsor's last update on 20 Sep 2018. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 5 sites in United States. 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.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was withdrawn before enrolling participants, so there are no results.
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-tonsillectomy bleeding within 14 days of surgery. (time frame: Within 14 days of surgery). 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 NCT03385057, which also lists 23 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 20 Sep 2018.