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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02970058
Other study ID # 01003060392
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 7, 2018
Est. completion date July 15, 2020

Study information

Verified date March 2019
Source Assiut University
Contact mohmed Bakri, prof
Phone +20882413201
Email mhbakri@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Platelet-rich Plasma Use as Prophylactic of Post-operative Low Back Pain Following gynecological surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date July 15, 2020
Est. primary completion date July 2020
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria:

- Elective gynecological surgery.

Exclusion Criteria:

- Spinal Pathology

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Platelet-rich Plasma
The active group will receive Platelet-rich Plasma following spinal injection
Control
The control group will receive saline as a placebo

Locations

Country Name City State
Egypt Assiut University Hospital Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analogue Scale 7 days