Effects of metamizol on postoperative pain in laparoscopic surgery in gynecology - a prospective application observation

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00012826

Enrollment

102

Registered

2018-01-29

Start date

2018-03-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

laparoscopic procedures, postoperative pain, gynecological patients

Interventions

Group 1: Adult patients of the gynecological clinic who undergo a laparoscopic procedure. It is documented whether patients receive metamizole intraoperatively or not. In addition, the severity of pai

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Female, from the age of 18, adequate knowledge of the German language, consentable, indication for a laparoscopic gynecological procedure

Exclusion criteria

Exclusion criteria: No consent, not consentable, male, age under 18 years, no laparoscopic gynecological intervention, intolerance to metamizole

Design outcomes

Primary

Measure	Time frame
Pain intensity measured using a numerical pain scale immediately after arrival in the recovery room	—

Secondary

Measure	Time frame
postoperative need for piritramid	—

Countries

Germany

Contacts

Public ContactAnnika Simon

Klinik für Anästhesiologie und Intensivmedizin, Medizinischen Hochschule Hannover

Simon.Annika@mh-hannover.de0511 532 0

Outcome results

None listed

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