Skip to content

Study for Comparison of Bloodloss, Range of motion and Functional Outcome in Total Knee Replacement with Tourniquet and without Tourniquet

Randomized Controlled Trial For Comparision Of Functional Outcome In Total Knee Replacement with Tourniquet and Without Tourniquet

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/05/014282
Enrollment
60
Registered
2018-05-31
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Patients with Osteoarthritis knee

Interventions

Intervention1: otal knee arthroplasty without using tourniquet under hypotensive spinal epidural anaesthesia: under hypotensive spinal epidural anaesthesia tourniquet will not be inflated. Control Int

Sponsors

All India Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients diagnosed with osteoarthritis scheduled for unilateral cemented TKA, either sex, aged <80 years

Exclusion criteria

Exclusion criteria: 1. Severe obesity. 2. Previous operation in concerning knee. 3. Lack of informed consent. 4. Severe cardiovascular conditions. 5. Patients receiving general anaesthesia during surgery.

Design outcomes

Primary

MeasureTime frame
Post-operative limb painTimepoint: Course of inpatient stay after total knee arthroplasty and follow up for 12 months

Secondary

MeasureTime frame
intra-and post-operative outcomes i.e. blood loss, SLRT, range of motion (ROM), deep vein thrombosis (DVT) in patients undergoing TKR.Timepoint: Blood Loss, measured by drain output at 6hr,24hr, and 48hr post operatively, drop in Hb and PCV at post operative day 0,day 1,day 7 and day 14,no.of patient require blood transfusion,safety assessed by B/L lower limb doppler at 7th post operative day ,6th week and 3rd month.;Radiolucency at bone cement interphase, knee society score.Timepoint: in follow up at 3 month, 6 month and 1 year.

Countries

India

Contacts

Public Contactswapnil singh

AIIMS, NEW DELHI

csyadavortho@gmail.com9868397115

Outcome results

None listed

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