Factors Influencing PAP and Its PM Among Patient Undergoing Elective Surgeries at Tertiary Care Hospital Mardan
NCT ID: NCT06768866
Last Updated: 2025-01-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ACTIVE_NOT_RECRUITING
386 participants
OBSERVATIONAL
2024-02-28
2025-03-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Comparison of Pain Scores by Using Audiovisual Aids.
NCT05452967
Improvement in Postoperative Pain Outcomes
NCT05624502
Postoperative Pain in Adult Patients.
NCT03731039
Direct Patient Feedback on Postoperative Pain
NCT05783440
Psychosocial Factors and Postoperative Pain in Aesthetic Breast Surgery
NCT06707818
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
RETROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Gruop 1
To determine factors influencing Postsurgical acute pain
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* ASA Class I,II are scheduled for elective surgeries under general anesthesia at Tertiary care hospital Mardan.
Exclusion Criteria
* 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"
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Superior University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Muhammad Naveed Babur
Principal Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Mardan Medical Complex
Mardan, Khyber Pakhtunkhwa, Pakistan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
MSAHS/Batch-Spring23/025
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.