Trans-perineal Trigger Point Dry Needling for Chronic Pelvic Pain

Dyspareunia Clinical Trial

Official title:

To Investigate the Use of Trans-perineal Trigger Point Dry Needling With Manual Therapy and to Compare the Outcome With Manual Therapy Treatment for Chronic Pelvic Pain With Dyspareunia. A Randomized Clinical Trial.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02795026
• Other study ID #: 115224510
• Status: Completed
• Phase: N/A
• Start date: April 2016
• Est. completion date: June 2018

Study information

• Verified date: September 2018
• Source: Cork University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Chronic Pelvic Pain (CPP) are around 10% of gynaecology referrals.Non-relaxing pelvic floor dysfunction (NRPFD) is an under-appreciated cause for CPP with dyspareunia where no other pathology exists. The effectiveness of manual therapy in studies have shown statistically significant pre and post treatment differences.However no study has reviewed the efficacy of inclusion of trans- perineal trigger point dry needling used with manual therapy for NRPFD. This study will investigate the effectiveness of trans-perineal trigger point dry needling used with manual therapy techniques for CPP.

Description:

This study will investigate the effectiveness of inclusion of trans-perineal trigger point dry needling with manual therapy treatment for chronic pelvic pain with dyspareunia and associated pelvic floor dysfunctions.The use of trigger point dry needling (TrptDN) for chronic low back pain has proved beneficial.This study will evaluate the treatment outcomes of trans-perineal trigger point dry needling and manual therapy to only manual therapy for CPP.

The outcomes will evaluate the number of treatment requirements between the dry needling with manual therapy group and the manual therapy group and review which group has faster resolution in pain and other associated pelvic floor symptoms.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 79
• Est. completion date: June 2018
• Est. primary completion date: April 2, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• Patients reporting non-cyclical CPP with dyspareunia and associated PFD with no palpable pelvic floor pathology, but with palpable high pelvic floor muscle (PFM) tone and tenderness will be referred for physiotherapy by the gynaecology team.

• Visceral conditions like interstitial cystitis are difficult to exclude at gynaecology review, as they mimic CPP symptoms.

• Smokers and non-smokers included.

• Nulliparous, singleton and multiparous patients.

Exclusion Criteria:

• Body mass index greater than 30, makes it difficult to dry needle as the required needle length is not available.

• Chronic back pain over 6 months duration, under pain management team.

• Orthopaedic back surgeries with implants.

• Pelvic pathologies like endometriosis, fibroids, cysts, etc.

• Pregnancy related pelvic pain.

• Pregnant during the trial.

• Pelvic organ carcinomas.

• Undergoing cancer treatment.

• Post gynaecology surgeries, less than 16 weeks.

• Cardiovascular, gastroenterology, renal or orthopaedic surgery, less than 6 month's post-operative.

• Neurological conditions like stroke, epilepsy, Parkinson's disease etc.

• Exclusion criteria for dry needling:

• Extreme needle phobia, Rheumatoid arthritis, prolonged corticosteroid treatment, warfarin treatment, heart implants and blood clotting disorders.

• Participant with no significant learning disability and should be able to understand the procedure to consent for treatment.

• Participant should not require a chaperone during treatment.

Related Conditions & MeSH terms

• Dyspareunia
• Pelvic Pain

Intervention

Procedure:
• Manual therapy
Myofascial trigger point release technique is a technique used to help ease tight muscles. This technique involves palpating the tight muscle for the 'knot'/trigger point and gently applying pressure for 30-60 seconds to help ease out the trigger point.
• Trigger point dry needling
Trigger point dry needling is a treatment technique involving the use of a single, disposable, fine filament acupuncture needle. Here the tight muscle is palpated and the acupuncture needle is directed towards the trigger point. The insertion of the needle is not felt, however the twitch reflex elicited to ease off the trigger point can be felt . This can be sore, but lasts only for a few seconds. Trans-perineal trigger point dry needling is an effective dry needling technique for the pelvic floor muscles done externally, targeting the trigger points in the pelvic floor muscles.

Locations

Country	Name	City	State
Ireland	Cork University Maternity Hospital	Cork	Co.Cork
Ireland	Cork Womens Clinic	Cork	Co.Cork

Sponsors (2)

Lead Sponsor	Collaborator
Cork University Hospital	University College Cork

Country where clinical trial is conducted

Ireland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain reduction or resolution within 10 treatment sessions, evaluated with the 0-10 Numeric Pain Rating Scale (0-10NPRS)	Participants will be asked to fill the 0-10NPRS at base line, 4th, 8th and 10th session or earlier on resolution of symptoms and to review which arm has faster resolution with lesser treatment sessions.	10 weeks or earlier on resolution
Secondary	Resolution in dyspareunia	Evaluated with the Female Sexual Functional Index questionnaire (FSFI) at baseline and the 10th session or earlier on resolution	10 weeks or earlier on resolution
Secondary	Resolution in bladder, bowel and sexual dysfunction	Evaluated with the abbreviated International Pelvic Pain Questionnaire (IPPQ) concentrating on dyspareunia and painful bladder and bowel symptoms. This is done at baseline and at 10th session or earlier as per resolution.	10 weeks or earlier on resolution
Secondary	Patient treatment satisfaction in each group	Evaluated with Pain Treatment Satisfaction Scale (PTSS) at 10th session or earlier on resolution	10 weeks or earlier on resolution