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Comparison of the effect of dexamethasone and ketorolac on pain control in elective foot surgery

Comparison of the effect of dexamethasone and ketorolac on pain control in elective foot surgery

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190304042908N2
Enrollment
40
Registered
2020-07-17
Start date
2020-06-21
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Patients who have lower limb orthopedic surgery.

Interventions

Intervention 1: Intervention group1: received 8 mg of dexamethasone intravenously. Intervention 2: Intervention group2: 90 mg of ketorolac (Caspian Tamin Rasht Company) was infused in 1 liter of norma

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: People who are candidates for lower limb orthopedic surgery. Be in the age range of 20 to 60 years.

Exclusion criteria

Exclusion criteria: Women who are pregnant and breastfeeding People with impaired renal function or dialysis People with heart disease, use of warfarin during treatment, People with contraindications to opioid medications People with gastrointestinal hemorrhage, history of high blood pressure People with history of anemia and thrombocytopenia People with drug addiction People with asthma and lung disease and allergies to NSAID.

Design outcomes

Primary

MeasureTime frame
Pain rate. Timepoint: Before injection and 2, 4, and 6 hours after the injection. Method of measurement: Visual Analog Scale VAS Pain: This scale represents the pain of patients in general. This scale is plotted as a 10-cm line, and the pain range is between 0 and 10 cm. The zero number does not show any pain, the number 1 to 3 mild pain, the number 4 to 6 average pain and the number 7 to 10 severe pain. The internal stability of this tool is 0.85. Up to 95 /. ROM: The neck flexion rate is measured using a goniometer. In this way, the goniometer axis is placed in the neck of the neck of the neck and on the proximal shoulder. The fixed arm is held along the horizons and movable arm along the longitudinal line of the neck, and the neck flexion range is asked from the person to move the neck forward without moving the head, and the angular changes are recorded.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahshid Ghasemi

Shahid Beheshti University of Medical Sciences

mahshidghasemi@sbmu.ac.ir+98 21 2243 2588

Outcome results

None listed

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