- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07357350
Effectiveness of Pain Management Interventions in Patients With Abdominal and Pelvic Cancer
January 15, 2026 updated by: Ali Sarfraz Siddiqui, Aga Khan University
Effectiveness of Pain Management Interventions in Patients With Abdominal and Pelvic Cancer in a Tertiary Care Hospital: A Prospective Observational Study
The goal of this prospective observational study is to observe the effectiveness of pain management interventions in patients with abdominal and pelvic cancer pain.
The main question[s] it aims to answer are:
- The effectiveness of pain management interventions.
- The frequency of pain intervention procedures and side effects and complications of pain management interventions
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ali Sarfraz Siddiqui, MBBS, FCPS
- Phone Number: 4397 00922134864397
- Email: sarfraz.siddiqui@aku.edu
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients with chronic pain due to abdominal and pelvic cancer.
Description
Inclusion Criteria:
- Patients with chronic pain due to abdominal and pelvic cancer
- Both Male and Female
- Ages18-65 years
- Patients who with recurrence or metastasis
Exclusion Criteria:
- Patients who refuse to give consent
- Patients who were lost to follow up after initial visit or assessment
- History of severe depression or psychiatric illness
- History of surgical procedure due to cancer
- Patients with DNR code
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient reported NRS score
Time Frame: First visit and then at 3 months
|
Numeric Rating Score from 0 (no pain)- 10 (severe pain)
|
First visit and then at 3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of patients
Time Frame: From 2 weeks to 3 months.
|
Number of patients on whom the intervention is performed.
|
From 2 weeks to 3 months.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
January 16, 2026
Primary Completion (Estimated)
October 15, 2026
Study Completion (Estimated)
December 31, 2026
Study Registration Dates
First Submitted
January 15, 2026
First Submitted That Met QC Criteria
January 15, 2026
First Posted (Actual)
January 22, 2026
Study Record Updates
Last Update Posted (Actual)
January 22, 2026
Last Update Submitted That Met QC Criteria
January 15, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- 2025-12177-38695
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Abdominal Cancer
-
M.D. Anderson Cancer CenterActive, not recruitingIntra-abdominal CancerUnited States
-
Assiut UniversityNot yet recruiting
-
Assiut UniversityNot yet recruiting
-
Assiut UniversitySouth Egypt Cancer InstituteCompletedPostoperative Analgesia | Lower Abdominal CancerEgypt
-
Tianjin Medical University Cancer Institute and...Tongji Hospital; The First Affiliated Hospital of Guangzhou Medical University and other collaboratorsCompletedThoracic Cancer | Abdominal CancerChina
-
Fayoum University HospitalCompleted
-
Assiut UniversityCompletedPain Relief in Upper Abdominal Cancer SurgeriesEgypt
-
Assiut UniversityNot yet recruitingQLB in Lower Abdominal Cancer Surgeries as a Post Operative Analgesia
-
University Health Network, TorontoRecruiting
-
The Netherlands Cancer InstituteCompleted