Skip to content

Effectiveness of Combination of Lidocaine and Ropivacaine on Analgesia and Anaesthesia characteristics in Costoclavicular Brachial plexus Block in Four Different Compositions.

To study the Effectiveness of Combining Lidocaine and Ropivacaine on the Duration of Analgesia and Anesthesia in Costoclavicular Brachial Plexus Block in Three Different Combinations. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/102225
Enrollment
96
Registered
2026-01-28
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: S523- Fracture of shaft of radius Health Condition 2: S529- Unspecified fracture of forearm

Interventions

Intervention1: Regional anesthesia: Group A Patients undergoing Costo clavicular block anaesthetised with 15ml 2% Lignocaine, Adrenaline[1:2lakh] with 15ml 0.75% Ropivacaine Control Intervention1:

Sponsors

Teerthanker Medical College and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients giving written and informed consent. American Society of Anesthesiologist (ASA) grade I-II of either sex. Age group of 18-70 years old. Planned for unilateral upper limb surgery.

Exclusion criteria

Exclusion criteria: pateints with coagulation and bleeding disorder local site infection any nerve injury history of allery to local anesthesia

Design outcomes

Primary

MeasureTime frame
To compare onset and duration of sensory block among the four groups. Timepoint: 30min, 2hrs, 4hrs, 6hrs, 8hrs, 12hrs, 16hrs, 20hrs, 24hrs.

Secondary

MeasureTime frame
To compare Numerical Rate Score [NRS] scale for pain post operatively. Timepoint: 30mins, 2hrs, 4hrs, 6hrs, 8hrs, 12hrs, 16hrs, 20hrs, 24hrs.

Countries

India

Contacts

Public ContactDr Payal Jain

Teerthankar Mahaveer Medical College and Research Centre

payalravi1408@gmail.com9855567933

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026