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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03108170
Other study ID # 3644
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 12, 2017
Est. completion date December 25, 2018

Study information

Verified date July 2020
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pregnant participants will be recruited at the obstetrics outpatient clinic during their visits 4 weeks before the due date. They are randomized into two groups. The first group will be educated to do digital perineal massage. They will be also educated to do pelvic floor muscle exercises and will receive the usual education program for strengthening the pelvic floor. The second group will receive the usual education program for strengthening the pelvic floor. Occurrence of perineal laceration will be reported at time of delivery.


Description:

Pregnant participants will be recruited at the obstetrics outpatient clinic during their visits 4 weeks before the due date. They are randomized into two groups. The first group will be educated to do digital perineal massage. They will be also educated to do pelvic floor muscle exercises and will receive the usual educational pelvic floor dysfunction prevention program for strengthening the pelvic floor. The second group will receive the usual education program for strengthening the pelvic floor. Occurrence of perineal laceration will be reported at time of delivery.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date December 25, 2018
Est. primary completion date December 20, 2018
Accepts healthy volunteers No
Gender Female
Age group 35 Years to 45 Years
Eligibility Inclusion Criteria:

- Pregnant women = 35 years old

- Primigravida or multi gravida

Exclusion Criteria:

- History of chronic constipation

- History of chronic cough

- Current or past urinary or anal incontinence

- History of genital prolapse before pregnancy

- History of neuromuscular disorders or connective tissue disorders

- History of medical disorders

- History of preterm or precipitate labour

- History of premature preterm rupture of membranes.

- Genital infections

Study Design


Related Conditions & MeSH terms


Intervention

Other:
perineal massage program
The participant will perform digital massage of her perineal area 5 minutes daily starting four weeks before delivery till her actual labour day
Pelvic floor muscle exercise program
The participant will perform pelvic floor muscle exercise daily starting four weeks before delivery till her actual labour day
Educational pelvic floor dysfunction prevention program
This educational pelvic floor dysfunction prevention program includes instructions about: control of her weight, adequate cleaning for the perineal area, adequate fluid intake, smoking cessation, right posture and frequency of micturition and adequate ingestion of fiber to avoid constipation

Locations

Country Name City State
Egypt Department of Obstetrics and Gynecology, Kasr Al-Ainy hospital Cairo Greater Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of participants who have perineal tears Proportion of perineal tears will be assessed by an investigator who will attend the participant delivery At 15 minutes from delivery
Secondary Proportion of participants who need episiotomy at time of delivery Proportion of participants who need episiotomy at time of delivery will be assessed by an investigator At 15 minutes from delivery
Secondary Duration of the second stage of labour Duration of the second stage of labour will be assessed by an investigator At 15 minutes from delivery
See also
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Completed NCT03559816 - Selective Use of Episiotomy: the Impact on Perineal Trauma.