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ACTIVE NOT RECRUITING
NCT06457581
NA

Effectiveness of Dry Needling Adjuvant to Selective Serotonin Reputake Inhibitors vs TP Injection for Pain Management

Sponsor: Superior University

View on ClinicalTrials.gov

Summary

The principal objective is to contribute valuable insights that hold direct implications for medical practice and patient care, with the potential to influence health policy pertaining to fibromyalgia management.

Official title: Effectiveness of Dry Needling Adjuvant to Selective Serotonin Reputake Inhibitors Versus Trigger Point Injection for Pain Management in Fibromyalgia

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

35

Start Date

2023-11-01

Completion Date

2024-09-30

Last Updated

2024-06-13

Healthy Volunteers

No

Interventions

OTHER

Dry Needling

Group A will undergo dry needling sessions twice a week over eight weeks, specifically targeting trigger points and tender points. Simultaneously, a consistent dosage of selective serotonin reuptake inhibitor (SSRI) will be administered and maintained throughout the entire duration of the study.

PROCEDURE

Trigger points injections

Group B will undergo a comprehensive intervention involving trigger point injections administered biweekly over eight weeks. These injections will specifically target trigger points. Additionally, a control measure will be implemented through simulated needling at non-specific points.

DRUG

serotonin reuptake inhibitor (SSRI)

serotonin reuptake inhibitor (SSRI)

Locations (1)

Chaudary Muhammad Akram Teaching Hospital

Lahore, Punjab Province, Pakistan