FindTrial
Sign In

Using a 5 percent Lignocaine Patch to Reduce Pain and Improve Satisfaction in Patients Receiving Spinal Anesthesia

Role of 5 percent Lignocaine Patch in Reducing Pain and Improving Patient Satisfaction During SpinalAnesthesia – An Observational Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/10/096220
Enrollment
60
Registered
2025-10-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: R688- Other general symptoms and signs

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

Dr Akshaya N Shetti
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults more than 18 years undergoing elective surgery under spinal anaesthesia. ASA physical status I–III. Provided written informed consent.

Exclusion criteria

Exclusion criteria: Known allergy to lignocaine or amide local anaesthetics. Skin lesions or infections at patch site. Contraindications to spinal anaesthesia.

Design outcomes

Primary

MeasureTime frame
Pain score at the site of spinal needle insertion measured using Visual Analogue Scale (VAS) immediately after spinal anesthesia. Timepoint: Baseline—

Secondary

MeasureTime frame
Incidence of local skin irritation or allergy at the site of patch application. Ease of spinal anesthesia performance as rated by the anesthesiologist (subjective 3 or 5 point scale).Timepoint: Baseline—

Countries

India

Contacts

Public ContactDr. Akshaya N. Shetti

Pravara Institute Of Medical Sciences, Loni, Ahmednagar, 413736

aksnsdr@gmail.com7385566253

Outcome results

None listed

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