FindTrial
Sign In

A CLINICAL TRIAL COMPARING LUMBAR PLEXUS BLOCK WITH EPIDURAL ANESTHESIA

USG GUIDED COMBINED LUMBAR PLEXUS -SCIATIC NERVE BLOCK VERSUS EPIDURAL ANAESTHESIA FOR LOWER LIMB ORTHOPEDIC SURGERY; A DOUBLE-BLINDED RANDOMIZED CONTROLLED TRIAL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/01/017312
Enrollment
80
Registered
2019-01-31
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: M958- Other specified acquired deformities of musculoskeletal system

Interventions

Intervention1: USG GUIDED COMBINED LUMBAR PLEXUS-SCIATIC NERVE BLOCK IN ONE GROUP: USG GUIDED COMBINED LUMBAR PLEXUS SCIATIC NERVE BLOCK WILL BE GIVEN USING A NERVE STIMULATOR NEEDLE AND INJECTION ROP

Sponsors

PGIMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: PATIENT IN AGE GROUP 18 TO 80 YR BOTH GENDERS AND ASA PHYSICAL STATUS 1-3 WILL BE TAKEN FOR STUDY IN INTERVENTION AND COMPARE GROUPS

Exclusion criteria

Exclusion criteria: A)PATIENT REFUSAL FOR EA OR UCSLB B)ALLERGY TO AMIDE LOCAL ANAESTHETIC DRUG C)CHRONIC OPIOID THERAPY D)PATIENT WHO CAN NOT UNDERSTAND NRS OR LINGUISTIC BARRIER E)PATIENT WITH THROMBOCYTOPENIA/COAGULOPATHY/ ANTI THROMBOLYTIC THERAPY F)MORBID OBESITY BMI >35 G)NEUROLOGICAL DISEASE H)INFECTION AT THE INTERVENTION SITE I)PATIENT WITH PSYCHIATRIC ILLNESS

Design outcomes

Primary

MeasureTime frame
TO COMPARE SUCCESS OF PROVIDING ADEQUATE ANAESTHESIA WITH COMBINED LUMBAR PLEXUS-SCIATIC NERVE BLOCK VERSUS EPIDURAL ANAESTHESIA IN ORTHOPEDIC LOWER LIMB SURGERYTimepoint: COMPLETE ANAESTHESIA, ADEQUATE FOR THE SURGERY WILL BE TESTED 15 YTO 20 MINUTES AFTER THE INJECTION OF LOCAL ANAESTHETIC—

Secondary

MeasureTime frame
1 hemodynamic changes 2 time of first analgesia request 3 time of onset of sensory block 4 time of onset of motor block 5 average pain 6 additional/ non opioid analgesic supplementation 7 incidence of adverse effect of LPSB 8 contralateral extension 9 motor block regression timeTimepoint: upto 48 hours follow up—

Countries

India

Contacts

Public ContactPARITOSH KUMAR AMAR

PGIMER CHANDIGARH

drtanvirsamra@yahoo.in7087008799

Outcome results

None listed

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