Dry Needling for Treating Spasticity in Multiple Sclerosis

NCT ID: NCT05351957

Last Updated: 2022-04-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-02-18

Study Completion Date

2020-09-22

Brief Summary

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The aim of the study is to evaluate the efficacy of dry needling (DN) in the treatment of spasticity in patients with multiple sclerosis (MS). \[Participants and Methods\] participants with MS, with no evidence of a relapse in the last four weeks and with an EDSS (Expanded Disability Sta- tus Scale) greater than 2.5 points (related with pyramidal score) were recruited. DN was performed in lower limbs for 12 consecutive sessions and evaluated with: EDSS (Pyramidal item), Time up and go (TUG), 25 foot, 9hold peg test (9HPT) and the improvement or not in the quality of life (MSQol54) was verified before and after treatment. A follow up visit was carried out to assess improvement.

Detailed Description

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Conditions

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Multiple Sclerosis

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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dry needling

This study has only 1 arm and the control group is their baseline data

Group Type EXPERIMENTAL

Dry needling

Intervention Type PROCEDURE

Only dry needling of the lower limbs will performed in all patients with acupunture needling

Interventions

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Dry needling

Only dry needling of the lower limbs will performed in all patients with acupunture needling

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Being a patient diagnosed with multiple sclerosis.
* Being over 18 years of age and less than or equal to 60 years of age.
* Having a score equal to or greater than 2 in the EDSS.
* They need to have a measurement in the following functional systems: P (pyramidal) \>2, CT (brainstem), gait \>2 and sphincter \>2.
* They need to present hypertonia or contractures of the muscles selected for the dry needling, the pain expressed by the patients must be a consequence of spastic processes, have hourly availability to receive therapies and not have needle phobias.

Exclusion Criteria

* Having a disease associated with multiple sclerosis that is incompatible with dry needling.
* Being in relapse, or having suffered it in the thirty days prior to starting the treatment. program or taking medications that are contraindicated with the technique applied in the study, (oral anticoagulants.)
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hospital Universitario de Canarias

OTHER

Sponsor Role lead

Responsible Party

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Alberto Javier Ormazábal

Physiotherapist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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MONSERRAT GONZÁLEZ-PLATAS

Role: STUDY_DIRECTOR

Hospital Universitario de Canarias

Locations

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Hospital Universitario de Canarias

San Cristóbal de La Laguna, Santa Cruz De Tenerife, Spain

Site Status

Countries

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Spain

Other Identifiers

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2017_100

Identifier Type: -

Identifier Source: org_study_id

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