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NCT04865523 Clinical Trial

Effectiveness of Manual Lymphatic Drainage in Patients With Fibromyalgia

Fibromyalgia Clinical Trial

— EMLDIPWF  

Official title:
Effectiveness of Manual Lymphatic Drainage in Patients With Fibromyalgia

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04865523
Other study ID # CamiloJcUFM
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 7, 2021
Est. completion date July 21, 2021

Study information
Verified date August 2023
Source Camilo Jose Cela University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Manual Lymphatic Drainage is a widely used technique for lymphedema. However, the analgesic effects of this technique could be potentially useful for managing pain in patients with generalized widespread chronic pain, including patients with fibromyalgia.

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date July 21, 2021
Est. primary completion date July 1, 2021
Accepts healthy volunteers No
Gender Female
Age group 30 Years to 55 Years
Eligibility Inclusion Criteria: - Women with diagnosis of Fibromyalgia. Exclusion Criteria: - Women with heart failure.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Manual Lymphatic Drainage
Manual lymphatic drainage is a technique that through gentle passes facilitates the flow of lymph through manual therapy techniques based on Vodder therapy. This technique is being studied to know its effectiveness in pain and for this reason we want to carry out this research.

Locations
Country Name City State
Spain Juan Antonio Valera-Calero Madrid

Sponsors (1)
Lead Sponsor Collaborator
Camilo Jose Cela University

Country where clinical trial is conducted

Spain, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain pressure threshold Kg/cm2 Baseline
Primary Pain pressure threshold Kg/cm2 Immediately after the intervention
Primary Pain pressure threshold Kg/cm2 Up to 15 days
Secondary Visual Analogue Scale 0-10 Baseline
Secondary Visual Analogue Scale 0-10 Immediately after the intervention
Secondary Visual Analogue Scale 0-10 Up to 15 days
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