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Postoperative pain control by topical subcutaneous analgesic injection at the end of surgery

Postoperative pain control by topical subcutaneous analgesic injection at the end of surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220108053667N1
Enrollment
100
Registered
2022-02-19
Start date
2022-01-08
Completion date
Unknown
Last updated
2022-03-08

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

Conditions

Pain control after surgery for ovarian malignancies. Malignant neoplasm of ovary

Interventions

Intervention 1: Intervention group: In the intervention group, at the end of surgery, before closing the skin in the subcutaneous area, 0.2% topical ropivacaine is injected at the rate of 1 to 2 cc pe

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients aged 40-60 years BMI = 25-30 without previous history of laparotomy ovarian mass with ultrasound, CT scan (solid cystic masses, papillary projection, abdominal ascites, parietal nodules, etc.) and tumor marker based on malignancy ( High levels of markers CA125 and CEA) laparotomy with midline incision average operation time of 60 to 90 minutes

Exclusion criteria

Exclusion criteria: History of severe heart disease anemia liver disease kidney disease anesthetic allergy history of hypotension or hypertension

Design outcomes

Primary

MeasureTime frame
Pain score of patients after surgery. Timepoint: 2, 6, 12 and 24 hours after surgery. Method of measurement: Patients' pain is measured based on Visual Analog Scale.

Secondary

MeasureTime frame
Recurrence of intestinal function. Timepoint: 12 and 24 hours after surgery. Method of measurement: Questions from the patient and patient file information.;Opioid use to control pain. Timepoint: 2,6,12,24 hours post operation. Method of measurement: patient file information.;Diclofenac suppository and acetaminophen injection for pain control. Timepoint: 2,6,12,24 hours post operation. Method of measurement: patient file information.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarjaneh Farazestanian

Mashhad University of Medical Sciences

FarazestanianM@mums.ac.ir+98 51 3840 0000

Outcome results

None listed

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