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Comparative study between standard palpatory method versus Ultrasound guided method for combined spinal epidural for patients undergoing Knee Replacement surgery

Comparative Study of Landmark versus Pre-Procedural Ultrasound Guided Combined Spinal Epidural Anaesthesia in Patients Undergoing Knee Arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015334
Enrollment
100
Registered
2018-08-14
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 undergoing surgery under spinal epidural anaesthesia

Interventions

Intervention1: nil: nil Intervention2: Ultrasound: Ultrasound guided CSE in TKR patients Control Intervention1: Landmark: Conventional landmark technique for TKR patients

Sponsors

Dr BL Kapur superspeciality hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Elective TKA â??CSE 2 50-75 years of age 3 ASA grade I - III

Exclusion criteria

Exclusion criteria: 1 Patients refusal 2 Patients belonging to ASA >= IV 3 Patients with contraindications for central neuraxial block - past history of spine surgery, infection focus at back, raised intracranial pressure and coagulopathy 4 Patients on anticoagulants or antiplatelet drugs 5 Patients with H/O allergy to the local anaesthetic

Design outcomes

Primary

MeasureTime frame
1. Number of attempts required for block in the same space 2. Number of inter-vertebral space changes required for the block 3. The depth at which epidural space was actually achieved versus that estimated with the pre-procedure ultrasound will be compared (In US group only Timepoint: All the primary outcomes will be assessed while doing the procedure i.e. during the ultrasound scanning and immediately after putting a successful CSE

Secondary

MeasureTime frame
1. Total duration of the procedure 2. Incidence of dural puncture in both the groups Timepoint: All the secondary outcomes will be assessed while doing the procedure i.e. during the ultrasound scanning and immediately after putting a successful CSE.

Countries

India

Contacts

Public ContactUmesh Kumar Valecha

Dr BLK Superspeciality Hospital

ukvalecha@gmail.com9810001903

Outcome results

None listed

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