Surgery-ComplicationsNCT06768866
Factors Influencing PAP and Its PM Among Patient Undergoing Elective Surgeries at Tertiary Care Hospital Mardan
An observational study of Surgery-Complications, run by Superior University at 1 site in Pakistan.
Trial summary
Postsurgical acute pain is a critical factor impacting recovery, patient satisfaction, and the risk of complications in surgical patients. Effective pain management is essential for enhancing patient outcomes and reducing the likelihood of chronic pain development. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Surgery-Complications
- What is being tested?
- Gruop 1
- Type of treatment
- Lifestyle or therapy programme
- How many people
- 386 participants
- Where
- 1 sitePakistan
- Study dates
- 28 Feb 2024to 1 Mar 2025
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
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 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: To determine factors influencing Postsurgical acute pain
Who may be able to join
- Patients with ages of 18 years and above.
- ASA Class I,II are scheduled for elective surgeries under general anesthesia at Tertiary care hospital Mardan.
Who cannot join
- Chronic opioid and NSAID user, tricyclic antidepressants and selective serotonin reuptake inhibitors.
- People with bleeding disorders.
- Postoperative respiratory depression, patient with emergency surgeries or admitted to ICU Postoperative.
- Procedure perform under regional Anesthesia, history of hypersensitivity to analgesic drugs and refusal to participate"
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Factors Influencing Postsurgical Acute Pain and Its Pharmacological Management Among Patient Undergoing Elective Surgeries at Tertiary Care Hospital Mardan
Postsurgical acute pain is a critical factor impacting recovery, patient satisfaction, and the risk of complications in surgical patients. Effective pain management is essential for enhancing patient outcomes and reducing the likelihood of chronic pain development.
Read the detailed description
However, pain perception is influenced by various factors, including demographic characteristics, types, duration and complexity of surgery, and pharmacological approaches. This study aims to identify these contributing factors and assess the effectiveness of different analgesics in managing postsurgical pain in a tertiary care setting.
- Conditions
- Surgery-Complications
- Being tested
- Gruop 1
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Gruop 1Behavioural
To determine factors influencing Postsurgical acute pain
What is being measured
The primary outcome is the main question the study is designed to answer.
Visual analog scale
Visual analog scale (0-10 VAS)and it was categorized using the following terms : no pain (0), mild (1-3), moderate (4-6),severe (7-9),or worse pain (10)
Measured: 12 Months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Jan 2025
- Study start28 Feb 2024
- Primary completion1 Jul 2024
- Study completion1 Mar 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Surgery-ComplicationsStudies of the same condition, open and under way.
- More trials run by Superior UniversityThe sponsor's other registered studies.
- 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
- Observational
- Observational model
- Case-control
- Time perspective
- Retrospective
- Enrolment
- 386 participants (actual)
Sponsor and investigators
- Lead sponsor
- Superior University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Muhammad Naveed Babur, Superior University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06768866
- Sponsor's protocol ID
- MSAHS/Batch-Spring23/025
- Status last verified
- Jan 2025
- First submitted
- 18 Dec 2024
- Last updated
- 10 Jan 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Jan 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Factors Influencing Postsurgical Acute Pain and Its Pharmacological Management Among Patient Undergoing Elective Surgeries at Tertiary Care Hospital Mardan
- ClinicalTrials.gov ID
- NCT06768866
- Acronym / sponsor ID
- MSAHS/Batch-Spring23/025
- Conditions
- Surgery-Complications
- Study type
- Observational
- Recruitment status
- Active, not recruiting
- Enrolment
- 386 participants (actual)
- Lead sponsor
- Superior UniversityUniversity, hospital or other
- Study start
- 28 Feb 2024 (actual)
- Primary completion
- 1 Jul 2024 (actual)
- Study completion
- 1 Mar 2025 (estimated)
- First posted
- 10 Jan 2025 (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.
Postsurgical acute pain is a critical factor impacting recovery, patient satisfaction, and the risk of complications in surgical patients. Effective pain management is essential for enhancing patient outcomes and reducing the likelihood of chronic pain development.
Detailed description
However, pain perception is influenced by various factors, including demographic characteristics, types, duration and complexity of surgery, and pharmacological approaches. This study aims to identify these contributing factors and assess the effectiveness of different analgesics in managing postsurgical pain in a tertiary care setting.
Study design
- Observational model
- Case-control
- Time perspective
- Retrospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- To determine factors influencing Postsurgical acute pain
Key inclusion criteria (2 listed)
- Patients with ages of 18 years and above.
- ASA Class I,II are scheduled for elective surgeries under general anesthesia at Tertiary care hospital Mardan.
Key exclusion criteria (4 listed)
- Chronic opioid and NSAID user, tricyclic antidepressants and selective serotonin reuptake inhibitors.
- People with bleeding disorders.
- Postoperative respiratory depression, patient with emergency surgeries or admitted to ICU Postoperative.
- Procedure perform under regional Anesthesia, history of hypersensitivity to analgesic drugs and refusal to participate"
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 |
|---|---|---|
| Gruop 1To determine factors influencing Postsurgical acute pain | Behavioural | – |
Primary outcome
Visual analog scale
Time frame: 12 Months
Visual analog scale (0-10 VAS)and it was categorized using the following terms : no pain (0), mild (1-3), moderate (4-6),severe (7-9),or worse pain (10)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Jan 2025.
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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?
An observational study of Surgery-Complications, run by Superior University 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 2 inclusion and 4 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: under way, not looking for participants, as of the sponsor's last update on 10 Jan 2025. 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?
This study is still under way. Results are not available in the source record yet.
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?
Visual analog scale (time frame: 12 Months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 10 Jan 2025.