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To determine the effectiveness combination of T12 paravertebral,lumbar plexus and sacral plexus blocks in hip surgeries.

A prospective observational study to determine the effectiveness of USG and PNS guided combination of T12 paravertebral,lumbar plexus and sacral plexus blocks in high risk patients undergoing hip surgeries - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/05/067541
Enrollment
30
Registered
2024-05-17
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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: Nil: Nil

Sponsors

Government medical College and new civil hospital surat
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients posted for hip orthopaedic surgeries receiving T12 paravertebral block along with combined lumbar and sacral plexus. Patients belonging to ASA grade 3/4 Patients giving written informed consent

Exclusion criteria

Exclusion criteria: 1.neuromuscular disease and established peripheral neuropathy 2.Skin infection at the site of needle insertion. 3.Chronic pain syndromes or receiving chronic analgesic therapy 4.Patients with reported history of allergy to any of the study drugs. 5.Patients having multiple fractures or having bilateral fractures

Design outcomes

Primary

MeasureTime frame
To observe , Time required to perform the block Onset and duration of motor and sensory block Quality of the block.Timepoint: To observe , Time required to perform the block Sensory evaluation will be done by pin prick with a 23 G needle an interval of 5,10,15,20,25 and 30 minutes. Motor block will be assessed at an interval of the 5, 10, 15, 20, 25 and 30 minutes. Motor block is graded on modified bromage scale Quality of the block.

Secondary

MeasureTime frame
Duration of postoperative analgesia & analgesic requirement in first 24hrs Hemodynamic changes Complications /adverse effect.Timepoint: At 2-hour, 4-hour, 8-hour, 12 hour & 24 hours after block.

Countries

India

Contacts

Public ContactDr Bansari N Kantharia

Government medical college,Surat

bansarikantharia@yahoo.com9825690177

Outcome results

None listed

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