Laparoscopy port-site wound infiltration Trial

Laparoscopy port-site wound infiltration with local anaesthetic for postoperative pain relief: A randomized controlled trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR201611001263105

Enrollment

200

Registered

2015-09-12

Start date

2015-09-12

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Fertility-male Post operative pain

Interventions

xylocaine group

Placebo

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: consent

Exclusion criteria

Exclusion criteria: Patients with known allergic reactions to local anaesthetics If the operation had been converted to an open procedure Patients with intra-operative complications. Chronic medical diseases Chronic opioid treatment.

Design outcomes

Primary

Measure	Time frame
1.Pain scores using a visual analogue scale. 2.Mortality.	—

Secondary

Measure	Time frame
1. Analgesic consumption 2. Time to first analgesic request. 3. Serious adverse events related to local anaesthetic wound infiltration such as allergic reactions, fits (convulsions), cardiac arrhythmias, and cardiac arrest.	—

Countries

Nigeria

Contacts

Public ContactCHIDIMMA OKAFOR

LIFE SPECIALIST HOSPITAL, LTD, NNEWI

donkafson@yahoo.com+2347030528420

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026