Effect of different touniquet pressure used during surgery,on post operative outcome after total knee replacement

A randomized controlled trial on the effect of different intraoperative tourniquet pressure on postoperative pain and complications after total knee replacement - nil

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/11/076582

Enrollment

Registered

2024-11-11

Start date

Unknown

Completion date

Unknown

Last updated

2024-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M171- Unilateral primary osteoarthritisof knee

Interventions

Intervention1: ALTERATION OF INTRA OPERATIVE TOURNIQUET BPRESSURE: PATIENTS TO BE ASSIGNED RANDOMLY,ACCORDING TO WHICH THEIR TOURNIQUET PRESSURE WILL BE THERE INTRAOPERATIVELY- 1.SYSTOLIC BP+80MMHG I

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients with OA knee planned for primary TKR (any side)in AIIMS PATNA 2.Age group 18 and above 3.Consenting participants

Exclusion criteria

Exclusion criteria: 1.Revision TKR. 2.Preop blood transfusion within 24hrs (PRBC only) 3.Evidence of recent Venous thromboembolism. 4.Contraindications for tourniquet use ( graft, peripheral vascular disease, calcified popliteals in xrays etc), cases where tourniquet is not used.

Design outcomes

Primary

Measure	Time frame
VAS score for pain Timepoint: 1.24hrs 2.48hrs 3.1 week	—

Secondary

Measure	Time frame
1.Knee Range of motion and VAS score for pain will be assessed 7 days after surgery.Timepoint: 1.Knee Range of motion and VAS score for pain will be assessed 7 days after surgery.	—

Countries

India

Contacts

Public ContactDr Arijit Keshri

AIIMS PATNA

drsudeepk@aiimspatna.org7765065667

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026