A clinical trial to evaluate the instillation of lignocaine during laparoscopc tubal ligation as a pain relief measure during and after surgery

PAIN RELIEF IN LAPAROSCOPIC TUBAL LIGATION USING INTRAPERITONEAL LIGNOCAINE: A DOUBLE BLIND RANDOMIZED CONTROLLED TRIAL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2009/091/000072

Enrollment

200

Registered

2009-03-06

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

None listed

Interventions

Intervention1: lignocaine: 20 ml of 0.5 % lignocaine Control Intervention1: isotonic saline: 20 ml

Eligibility

Inclusion criteria

Inclusion criteria: All women who desired laparoscopic sterilization under local analgesia and sedation were included in the study

Exclusion criteria

Exclusion criteria: known hypersensitivity to local anesthetics, history of seizures or known cardiac or renal disease

Design outcomes

Primary

Measure	Time frame
Pain score was measured using visual analogue scale (VAS)Timepoint: Pain score measured intra operatively during manipulation of tubes and Falope ring application and post operatively at 0.5 hours, one hour and three hours.	—

Secondary

Measure	Time frame
Post operative nausea, vomiting and any symptoms of lignocaine toxicity were also recordedTimepoint: 6 hours	—

Countries

India

Contacts

Public ContactSreekumarn Nair

consultant

drnidhu@yahoo.com09216313113

Outcome results