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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05774067
Other study ID # tourniquet deflation
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 1, 2022
Est. completion date July 30, 2023

Study information

Verified date November 2023
Source Tanta University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pneumatic tourniquet is usually used in orthopedic surgeries, as it helps to decrease operative bed bleeding, and thus, maintaining a clean and dry surgical field allowing easy and clear identification of the anatomical structures. Despite that advantage, after its deflation, there is a blood volume shift towards that ischemic area, which may decrease cardiac preload leading to hypotension


Description:

Hemodynamic changes after tourniquet deflation include; hypotension, tachycardia and increase in cardiac index. These changes may be insignificant for healthy individuals but, risky for patients with compromised cardiovascular system and geriatric population. Hypovolemia is a common problem in many clinical situations. The mortality of hypovolemic shock is directly related to the severity and duration of organ hypoperfusion. Management of hypotension include frequent monitoring of blood pressure, fluid therapy, non-pharmacological methods, and vasopressors. Fluid therapy by crystalloids or colloids has been the traditional approach to restore volume and can be given as preload or co-load .Non pharmacological methods include positioning and leg compression. Trendelenburg position can increase venous return to the heart. Leg compression by flexion of the hip, elastic bandages, or stockings. An efficient method to treat spinal hypotension is administration of vasopressors, either given by infusion or boluses. Vasopressor drugs act by reversing the circulatory effect of sympathetic blockade. They also restore vascular tone and preserve venous return and cardiac filling


Recruitment information / eligibility

Status Completed
Enrollment 135
Est. completion date July 30, 2023
Est. primary completion date June 30, 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years to 65 Years
Eligibility Inclusion Criteria: - Adult Patients of both gender - American Society of Anesthesiologists (ASA) I or II - scheduled for elective unilateral total knee arthroplasty Exclusion Criteria - Patient refusal. - Major cardiopulmonary disorders - Uncontrolled systemic hypertension. - Hepatic or renal disorders. - Patient with relative contraindication for tourniquet use as peripheral vascular disease, sickle cell anemia, deep venous thrombosis, diabetic neuropathy and crushed injury. - Cases having American Society of Anesthesiologists [ASA] > II - Coagulopathy and bleeding tendency. - Revision knee arthroplasty and bilateral knee arthroplasty

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Saline
patient received normal saline 4ml/kg/hr with deflation of tourniquet
Norepinephrine
patient received noradrenaline infusion at rate 0.1 mcg/kg/min. with deflation of tourniquet
glypressin
patient receive glypressin infusion at rate 2 mcg/kg/hr.

Locations

Country Name City State
Egypt Faculty of medicine, Tanta university Tanta El Gharbyia

Sponsors (1)

Lead Sponsor Collaborator
Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary change of mean arterial blood pressure change of mean arterial bllod pressure till 30 min after deflation of the tourniquet. 30 minutes after tourniquet deflation
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