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RECRUITING
NCT06286540
NA

Evaluation of the Efficacy and Safety of Surgical Device "Lymphoblock" for Prevention of Lymphorrhea in Patients With Thoracoabdominal Aorta Repair.

Sponsor: Petrovsky National Research Centre of Surgery

View on ClinicalTrials.gov

Summary

Randomized, double-blind, placebo-controlled study will determine the clinical efficacy and safety of Lymphoblock in the prevention of postoperative retroperitoneal chylo-/lymphorrhoea in patients with open surgical treatment of the thoracoabdominal aorta. It is planned to recruit 138 clinical observations. Efficacy will be evaluated based on clinical and laboratory data.

Official title: Efficacy and Safety of Lymphoblock in the Prevention of Postoperative Lymphorrhea After Surgical Treatment of the Thoracoabdominal Aorta: a Single-center, Randomized, Placebo-controlled, Double-blind Study.

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

138

Start Date

2023-02-22

Completion Date

2026-05

Last Updated

2024-03-15

Healthy Volunteers

No

Interventions

DEVICE

Lymphoblock

1 time per surgery with the exposition for 20 minutes.

DEVICE

Placebo

1 time per surgery with the exposition for 20 minutes.

Locations (1)

Petrovsky NRCS

Moscow, Russia