The Use of Local Hemostatic in Patients With Large Incisional Hernias

Status Completed

Clinical Trial Summary

Design of a simple blind randomized controlled trial study. Large incisional hernia repair with use of local hemostatic Hemoblock

Clinical Trial Description

Design of a simple blind randomized controlled trial study. The total number of subjects was 66. In the main group (A) - 33, in the other group (B) - 33. Operation - sublay retromuscular using prolene mesh implant. In group A Hemoblock 15 ml in the retromuscular and 15 ml in the subcutaneous spaces were used. Wounds were drained by vacuum-suction drainage. Postoperative monitoring of early ultrasound examinations on the 3rd, 7th, 10th, 12th, 15th, 18th, 21st, 25th, 28th, 30th days after drainage removal.

In group B were used a standard intervention (sublay retromuscular). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04222517
Study type	Interventional
Source	Nijznevartovsk County Clinical Hospital
Contact
Status	Completed
Phase	N/A
Start date	September 10, 2017
Completion date	January 4, 2020

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