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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02775747
Other study ID # PRP-CS
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received May 7, 2016
Last updated May 12, 2017
Start date April 2016
Est. completion date April 2017

Study information

Verified date April 2016
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There is limited application of the use of PRP in obstetrics, therefore there is a need for assessment if it is efficacy in improving skin wound healing in cesarean section.


Description:

This study aims to assess the efficacy of injection of platelet rich plasma into the wound of recurrent cesarean section for improving wound healing and enhancing the shape of the wound in women undergoing cesarean section.


Recruitment information / eligibility

Status Completed
Enrollment 128
Est. completion date April 2017
Est. primary completion date March 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 25 Years to 35 Years
Eligibility Inclusion Criteria:

- elective cesarean section

- Body mass index 18:25

- Hemoglobin more than 10.5 g/d

- Albumin within normal more than or equal 3.5 g/d

Exclusion Criteria:

- medical disorders(Diabetes mellitus,heart disease,hypertension,systemic lupus erythematosus)

- high risk pregnancy as (placenta previa,placenta accreta)

- patient on corticosteroids medication

- primigravida subjected cesarean section

- complicated cesarean section (increased operation time,blood transfusion, drain, scrubbing of multiple surgeons)

- cesarean section due to chorioaminionitis

- postoperative complication such as:postpartum hemorrhage, paralytic ileus, sever distention..) will be dropped out from the study

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
platelet rich plasma gel
Platelet rich plasma is prepared from fresh whole blood which is collected from a peripheral vein stored in acid citrare dextrose solution A (ACD-A)anticoagulant and processed to increase platelets by separating various components of blood
saline
64 controlled women with recurrent cesarean section and fullfit to all inclusion and exclusion craiteria will reseve saline injection at time of wound closure

Locations

Country Name City State
Egypt Rasha Cairo Al Qahirah

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Efficacy of PRP in Wound healing in cesarean section by 100 mm visual analog scale Efficacy of PRP in Wound healing in cesarean section by 100 mm visual analog scale (VAS) for wound healing one month
Secondary Assessment of the Cosmetic results of the wound by Modified Vancouver scar scale Assessment of the Cosmetic results of the wound by Modified Vancouver scar scale one month
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