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Comparison of pain after abdominal surgery in patients receiving ketorolac and nasocalcin spray or lidocaine and nasocalcin spray

Comparison of pain after abdominal surgery in patients receiving ketorolac and nasocalcin spray or lidocaine and nasocalcin spray

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230710058733N1
Enrollment
59
Registered
2023-09-26
Start date
2021-09-20
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Pain after abdominal surgery. Unspecified complication of procedure

Interventions

Intervention 1: 2 puffs of nasocalcin and Ketorolac 30 mg ampoules were received intravenously. After patients enter the operating room, patients under general anesthesia with the same drugs (propofol

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 75 Years

Inclusion criteria

Inclusion criteria: Being 15-75 years old Sign a personal consent form to enter the study American Society of Anesthesiologists 1-2 Non-use of drugs and alcohol Elective surgery

Exclusion criteria

Exclusion criteria: Decreased level of consciousness Hemodynamic disorder Abnormal intraoperative bleeding Length of operation more than 4 hours

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 1 hour and 6, 12, 24 hours after the operation, the amount. Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
The amount of narcotic (pethidine) received after the operation. Timepoint: After surgery. Method of measurement: Amount of drug used.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mahnaz Narimani Zamanabadi

Islamic Azad University

Mahdieh.ir72@yahoo.com+98 21 7719 0836

Outcome results

None listed

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