NCT07357350

Brief Summary

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

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
8mo left

Started Jan 2026

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress32%
Jan 2026Dec 2026

First Submitted

Initial submission to the registry

January 15, 2026

Completed
1 day until next milestone

Study Start

First participant enrolled

January 16, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

January 22, 2026

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 15, 2026

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

January 22, 2026

Status Verified

January 1, 2026

Enrollment Period

9 months

First QC Date

January 15, 2026

Last Update Submit

January 15, 2026

Conditions

Abdominal Cancer

Outcome Measures

Primary Outcomes (1)

  • Patient reported NRS score

    Numeric Rating Score from 0 (no pain)- 10 (severe pain)

    First visit and then at 3 months

Secondary Outcomes (1)

  • Number of patients

    From 2 weeks to 3 months.

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with chronic pain due to abdominal and pelvic cancer.

You may qualify if:

  • Patients with chronic pain due to abdominal and pelvic cancer
  • Both Male and Female
  • Ages18-65 years
  • Patients who with recurrence or metastasis

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Ali Sarfraz Siddiqui, MBBS, FCPS

CONTACT

00922134864397sarfraz.siddiqui@aku.edu

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

January 15, 2026

First Posted

January 22, 2026

Study Start

January 16, 2026

Primary Completion (Estimated)

October 15, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

January 22, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share