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The effect of lidocaine on pain after abdominal hysterectomy surgery

The effect of Intraperitoneal lidocaine on pain after abdominal hysterectomy

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201207021306N6
Enrollment
40
Registered
2012-07-18
Start date
2007-06-17
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Single delivery by caesarean section. O82.0

Interventions

Intervention 1: At the end of operation number1 solution(50cc of 0.9% normal saline ) infiltrated within peritoneal cavity and then abdomen was closed. Intervention 2: At the end of operation numbe
Treatment - Drugs
At the end of operation number1 solution(50cc of 0.9% normal saline ) infiltrated within peritoneal cavity and then abdomen was closed
At the end of operation number 2 solution( 50cc of lidocain 0.8% plus epinephrine 1/50000) was infiltrate to the peritoneal cavity and then abdomen was closed

Sponsors

Vice chancellor for research-Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: The exclusion criteria are: positive history of hepatits; cardiovascular diseases; hypersensitivity to local analgesic agents; history of conclusion; asthma; addiction; cancer and concomitant surgeries. Inclusion criterion: all patient who are candidate for abdominal of hysterectomy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Evaluation of Pain. Timepoint: At hours 8, 12, 24 and 48 hours after surgery and after surgery at the time of movement. Method of measurement: Visual pain scale.

Secondary

MeasureTime frame
Side effects (dizziness, vomiting, nausea). Timepoint: Within 24 hours after surgery. Method of measurement: By Assistant.;Dosage of drugs. Timepoint: Within 24 hours after surgery. Method of measurement: By Assistant.;Satisfaction levels. Timepoint: Within 24 hours after surgery. Method of measurement: Ask the patient.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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