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An observational study on patient satisfaction and effectiveness of ultrasound-guided anesthesia for arm and hand surgeries.

Patient satisfaction and effectiveness of ultrasound-guided regional anesthesia for upper limb surgeries: A cross-sectional observational study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/11/097945
Enrollment
60
Registered
2025-11-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Nil: No experimental or comparator intervention is involved. All participants receive standard-of-care ultrasound-guided regional anesthesia for upper limb surgeries. Data will be coll

Sponsors

Vinayaka Missions Kirupananda Variyar Medical College and Hospitals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients undergoing upper limb surgeries under ultrasound guided regional anesthesia 2. Age group: 18 to 60 years 3. American Society of Anesthesiologists Physical Status (ASA-PS) I, II and III 4. Both male and female patients 5. Patient providing written informed consent

Exclusion criteria

Exclusion criteria: 1. Patient refusal or inability to provide informed consent 2. Age less than 18 or more than 60 years 3. American Society of Anesthesiologists Physical Status (ASA-PS) IV or higher 4. Obstetric patients 5. Psychiatry patients

Design outcomes

Primary

MeasureTime frame
To evaluate the effectiveness of ultrasound-guided regional anesthesia for upper limb surgeries by assessing the intraoperative need for supplemental analgesic and/or sedative medication or the conversion to general anesthesia.Timepoint: Use of supplemental analgesic and/or sedation or conversion to general anaesthesia recorded at end of surgery.

Secondary

MeasureTime frame
To assess patient satisfaction with their nerve block postoperatively. To evaluate the duration of postoperative analgesia provided by the nerve block. To determine the incidence of complications or adverse effects related to ultrasound-guided regional anesthesia.Timepoint: Patient satisfaction of the nerve block will be assessed postoperatively at 4 hours and 8 hours post procedure. Patients pain level will be assessed immediately(0 minutes), 2 hours, 4 hours and 8 hours postoperatively. Adverse events and complications will be assessed immediately(0 minutes), after 1 hour, 4 hours and 8 hours post procedure.

Countries

India

Contacts

Public ContactDr Ajin Arul David

Vinayaka Missions Kirupananda Variyar Medical College and Hospitals

sabapathyv.appavoo@gmail.com9442566989

Outcome results

None listed

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