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Total Knee Arthroplasty With and Without Tourniquet: Comparative Study

H

Hawler Medical University

Status

Completed

Conditions

Total Knee Arthroplasty

Treatments

Procedure: Tourniquet use

Study type

Interventional

Funder types

Other

Identifiers

NCT04130009
HMU/Sherwan4

Details and patient eligibility

About

Tourniquet use during total knee arthroplasty (TKA) improves visibility and reduces intraoperative blood loss. However, tourniquet use may also have a negative impact on early recovery of muscle strength and lower extremity function after TKA.Seventy Patients are involved in this study and were divided into two groups; Group A (35) patients were treated with TKA with pneumatic thigh tourniquet. Group B (35) patients were treated with TKA without tourniquet. All patients were suffering from severe knee osteoarthritis and they failed to respond to conservative treatment so they are candidates for primary TKA. The two groups are matched related to age and gender. Selection of patients into two groups done randomly with regard of odd number for group A and even number for group B

Full description

This study started on March 2016 and ends on October 2018. Seventy Patients are involved in this study and were divided into two groups; Group A (35) patients were treated with TKA with pneumatic thigh tourniquet. Group B (35) patients were treated with TKA without tourniquet. All patients were suffering from severe knee osteoarthritis and they failed to respond to conservative treatment so they are candidates for primary TKA. The two groups are matched related to age and gender. Selection of patients into two groups done randomly with regard of odd number for group A and even number for group B. All patients were followed for a period of two weeks until removal of skin sutures for the following parameters:

Amount of blood transfusion done at and after surgery. Amount of blood drained postoperatively through suction drain. Occurrence of postoperative wound hematoma. VAS (Visual analogue score) for thigh pain at 1st day and (2) weeks postoperatively.

Clinical DVT.

Enrollment

70 patients

Sex

All

Ages

48 to 82 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients were suffering from severe knee osteoarthritis and they failed to respond to conservative treatment

Exclusion criteria

  • Hb less than 12.
  • D.M.,Blood dyscrasia.
  • Any evidence of infection by screening test ESR and CRP. ,
  • BMI more than 30.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

70 participants in 2 patient groups

TKA with tourniquet
Active Comparator group
Description:
This group was treated by TKA with the use of tourniquet
Treatment:
Procedure: Tourniquet use
TKA without tourniquet
Active Comparator group
Description:
This group was treated by TKA without tourniquet
Treatment:
Procedure: Tourniquet use

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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