Clinical Trials Directory

Trials / Completed

CompletedNCT03159871

Closing Uterine Incision During C-section Using Barbed Suture (Stratafix) or Vicryl Suture.

Closing Uterine Incision During C-section Using Barbed Suture (Stratafix) or Vicryl Suture: a Randomized Control Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
73 (actual)
Sponsor
Barzilai Medical Center · Academic / Other
Sex
Female
Age
18 Years – 42 Years
Healthy volunteers
Accepted

Summary

A Randomized prospective single blinded trial. The investigator seek to evaluate the surgical outcome of Stratafix barbed suture compared to standart Vicryl sutures in reducing the suturing time during C-Section.

Detailed description

A Randomized prospective single blinded trial. The investigator seek to evaluate the surgical outcome of Stratafix barbed suture compared to standart Vicryl sutures in reducing the suturing time during C-Section. In addition, the need of additional sutures to control bleeding after the 2- layer closure will be estimated.These will be the primary outcome measures. The secondary outcome measures will be factors related to the blood loss at the time of the uterine closure, surgical complications, duration of hospital stay, postoperative infection (endometritis) and wound infection..

Conditions

Interventions

TypeNameDescription
DEVICEStratafix sutureStratafix barbed sutures during C-Sections.
DEVICEVicryl sutureStandart Vicryl suture during C- Sections.

Timeline

Start date
2016-06-29
Primary completion
2017-12-21
Completion
2017-12-24
First posted
2017-05-19
Last updated
2018-05-31

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT03159871. Inclusion in this directory is not an endorsement.