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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05885945
Other study ID # TC-01/23
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 15, 2023
Est. completion date July 31, 2023

Study information

Verified date January 2024
Source Catholic University of Murcia
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Analysis of stabilometric and respiratory variables in patients with dysmenorrhea during the first day of the menstrual cycle and any other day outside the cycle.


Description:

Sociodemographic variables such as age, height, body mass index. Respiratory variables such as maximum inspiratory pressure (MIP), MIP reference %, and MIP predictive value. Stabilometric variables we will measure the balance in condition of eyes open and eyes closed bipodal support and eyes open in monopodal support


Recruitment information / eligibility

Status Completed
Enrollment 23
Est. completion date July 31, 2023
Est. primary completion date June 14, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Adult women with primary dysmenorrhea. - Not having had any type of childbirth (natural, caesarean section, etc). - Not be positive in COVID. Antigen test in the last 24 hours or negative PCR in the last 48 hours. Exclusion Criteria: - Receive medical treatment during research. - Have any orthopedic, neurological or systemic disease diagnosed other than primary dysmenorrhea. - Be in follow-up with any medical treatment that does not be primary dysmenorrhea - Women with a history of trauma or surgical treatment who involve the musculoskeletal system in the last year. - Use of analgesics in the last 48 hours. - Consumption of alcohol in the last 24 hours. - Have a history or suspicion of pregnancy.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Spain University Catholic of Murcia Guadalupe Murcia

Sponsors (1)

Lead Sponsor Collaborator
Catholic University of Murcia

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Balance stabilometric variables in bipodal and monopodal support 2 months
Primary diaphragmatic muscle strength diaphragmatic muscle force through the maximum inspiratory pressure in the mouth 2 months
Secondary sociodemographic variables sociodemographic variables such as age, body mass index, personal data record, and data record related to pain and dysmenorrhea 2 monsths
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