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A study to Investigate the Effect of Intraperitoneal Levobupivacaine on Post Operative Laparoscopic Pain - LAPLIQUID study

A study to Investigate the Effect of Intraperitoneal Levobupivacaine on Post Operative Laparoscopic Pain - LAPLIQUID study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2009-011207-23-GB
Enrollment
108
Registered
2009-09-17
Start date
2009-08-05
Completion date
Unknown
Last updated
2019-06-30

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

Conditions

Post operative pain

Interventions

Trade Name: Chirocaine Product Name: Chirocaine Pharmaceutical Form: Injection* INN or Proposed INN: LEVOBUPIVACAINE CAS Number: 2726247

Sponsors

Hull and east Yorkshire Hospital NHS Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria will be all women about to undergo minor laparoscopic surgery. Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: Exclusions will be women with a BMI>35 or with an ASA >2, known previous adverse reaction or any contraindication to levobupivacaine. It is also necessary to exclude women who have a painful condition immediately prior to the surgery.

Design outcomes

Primary

MeasureTime frame
Main Objective: The principle research question is whether leaving a local anaesthetic solution in the abdomen after keyhole surgery improves pain relief.;Secondary Objective: Secondary research questions are whether leaving a local anaesthetic solution in the abdomen after keyhole surgery reduces the need for other pain killing agents and reduces the duration of hospital stay.;Primary end point(s): The pain score in the evening after surgery.(8hours)

Countries

United Kingdom

Outcome results

None listed

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