CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 43 enrolled
Drug / intervention
Surgicel Snow +1 moredevice
Likely dose
Not stated in record
Key inclusion· 3
  • Women aged 18 years or older
  • Scheduled for laparoscopic hysterectomy (standard multiport, single site, or robotic-assisted)
  • Surgery for benign, complex benign, or malignant indications
Key exclusion· 5
  • Vaginal or open abdominal hysterectomy
  • Congenital or acquired coagulation disorder
  • Therapeutic anticoagulation or antiplatelet agents (other than low-dose aspirin) within 7 days of surgery
  • Hysterectomy concurrent with sacrocolpopexy

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02908841
NCT02908841N/ACompleted

Surgicel Snow in Gynecological Surgery

Danbury Hospital·interventional·Posted Sep 21, 2016·Updated Jul 14, 2021

In Brief

A clinical study evaluating Surgicel Snow and Standard of Care for Laparoscopic Hysterectomy. Completed, enrolled 43 participants across 3 sites.

Detailed Summary

Surgicel Snow is an FDA approved topical hemostatic agent for use during surgical procedures. Like the other mechanical agents, Surgicel Snow forms a physical barrier that blocks blood flow while providing a large surface area for the rapid formation of a fibrin clot. As a mechanical agent derived from oxidized regenerated cellulose, Surgicel Snow shares with other mechanical hemostatic agents, the benefits of a favorable risk profile. This study would examine the efficacy of Surgicel Snow vs. direct compression in the control of capillary, venous, and small arterial hemorrhage when ligation or other conventional methods of control are impractical or ineffective in patients undergoing laparoscopic or robotic assisted laparoscopic hysterectomy. The intraoperative inclusion bleeding characteristics are minimal and mild retroperitoneal bleeding and moderate retroperitoneal bleeding that has been adequately reduced by standard surgical methods. 60 patients will be recruited for this study, all of which will be scheduled for hysterectomy at Western Connecticut Health Network (Norwalk Hospital and Danbury Hospital) under the direction of Dr. Thomas Rutherford, Dr. John Garofalo, and Dr. Robert Samuelson. The investigators will randomize 30 patients to the treatment group and 30 patients to the control group. Participants may continue all regular medications before and during the study. The consent process will be incorporated into the last pre-operative office visit. The health risks associated with use of Surgicel Snow may be less, the same or more than direct pressure alone. Surgicel Snow is generally used for minimal to mild bleeding from specific or widespread area; however, its effectiveness compared to direct pressure is unknown for a hysterectomy surgery.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsEthicon, Inc.

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedSep 21, 2016
Enrollment StartJul 1, 2016
Primary CompletionSep 1, 2018
Study CompletionFeb 11, 2019
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 9.8 years ago

Interventions

Surgicel Snowdevice

Standard of Careother