Effectiveness of Pain Management Interventions in Patient... | NCT07357350

Studies
Effectiveness of Pain Management Interventions in Patients With Abdominal and Pelvic Cancer

NCT07357350

Sponsor

Aga Khan University

Status

Not yet recruiting

Last Update Posted

Jan 22, 2026Actual

Enrollment

100Estimated

Phase

Not provided

Conditions

Abdominal Cancer

Interventions

Not provided

Countries

Not provided

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Jan 2026

Overall Recruitment Status or Expanded Access Status

Not yet recruiting

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Jan 16, 2026Estimated

Primary Completion Date

Oct 15, 2026Estimated

Completion Date

Dec 31, 2026Estimated

First Submitted Date

Jan 15, 2026

First Submission Date that Met QC Criteria

Jan 15, 2026

First Posted Date

Jan 22, 2026Actual

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Jan 15, 2026

Last Update Posted Date

Jan 22, 2026Actual

Oversight Module

Has Data Monitoring Committee (DMC)

Is FDA Regulated Drug

Is FDA Regulated Device

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

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

Detailed Description

Not provided

Design Module

Study Type

Observational

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Target Follow-Up Duration

Not provided

Phases

Not provided

Interventional Study Design

Allocation

Not provided

Intervention Model

Biospecimen

No data available

No data is available for this block.

Enrollment

100Estimated

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Patient reported NRS score	Numeric Rating Score from 0 (no pain)- 10 (severe pain)	First visit and then at 3 months

Secondary Outcomes

Measure	Description	Time Frame
Number of patients	Number of patients on whom the intervention is performed.	From 2 weeks to 3 months.

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

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

Accepts Healthy Volunteers

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

18 Years

Maximum Age

65 Years

Standard Ages

AdultOlder Adult

Study Population

Patients with chronic pain due to abdominal and pelvic cancer.

Sampling Method

Non-Probability Sample

Contacts/Locations Module

Central Contacts

Name	Role	Phone	Extension	Email
Ali Sarfraz Siddiqui, MBBS, FCPS	Contact	00922134864397	4397	sarfraz.siddiqui@aku.edu

Overall Officials

Not provided

Locations

Not provided

IPD Sharing Statement Module

Plan to Share IPD

Description

Not provided

Types

Not provided

Time Frame

Not provided

Access Criteria

Not provided

URL

Not provided