ClinicalTrials.Veeva

Menu

Extracorporeal Shock Wave Therapy for Dysmenorrhea

M

MTI University

Status

Completed

Conditions

Primary Dysmenorrhea

Treatments

Other: shock wave therapy
Other: dietary modification

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

purpose of this study to investigate the effect of Extracorporeal shock wave therapy on pain and prostaglandin level in patient with primary dysmenorrhea

Full description

This randomized controlled trial is to determine the effect of shock wave therapy in the treatment of primary dysmenorrhea.

females are randomly assigned into 2 groups: group A SWT treatment plus dietary modification during PD (n=25) GROUP B:dietary modification only (n=25);

Participants in group B will receive dietary modification for three successive months

The numerical rating scale (NRS) and prostaglandin blood level will be recorded and evaluated before and after treatment.

Enrollment

50 patients

Sex

Female

Ages

18 to 25 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. ages ranged between18 - 25 years old.
  2. body mass index (BMI) will not exceed 30kg/m2.
  3. females will be diagnosed by the physician as primary dysmenorrhea.

Exclusion criteria

  1. Secondary dysmenorrhea .
  2. Mental health problem such as depression and anxiety.
  3. Irregular periods

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

shock wave
Experimental group
Description:
shock wave for primary dysmenorrhea for study group along side to dietary modification
Treatment:
Other: dietary modification
Other: shock wave therapy
dietary modification
Active Comparator group
Description:
dietary modification for primary dysmenorrhea for control group
Treatment:
Other: dietary modification

Trial documents
1

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems