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Reduction of post-operative pain using intravenous acetaminophen, ketamine and tramadol in open renal surgeries

Comparison of analgesic effect of intravenous acetaminophen and ketamine versus intravenous acetaminophen and tramadol in patients undergoing open renal surgeries

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201509143773N14
Enrollment
60
Registered
2016-02-07
Start date
2015-10-21
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

post operation pain. Pelvic and perineal pain

Interventions

Intervention 1: First intervention group: intravenous acetaminophen 1gr and tramadol 0.7mg/kg will be administered At the end of surgery. Intervention 2: Second intervention group: intravenous acetami
Treatment - Drugs
First intervention group: intravenous acetaminophen 1gr and tramadol 0.7mg/kg will be administered At the end of surgery.
Second intervention group: intravenous acetaminophen 1gr and ketamine 0.5mg/kg will be administered at the end of surgery .

Sponsors

Vice chancellor for research,Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Older than 18 years old; With ASA I & II. Exclusion criteria: patients with the history of opium use; history of psychological disorders; chronic low back pain.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 5, 10, and 20 minutes after arriving to the recovery room, to the ward, and also 1 and 6 hours after transfer to the ward. Method of measurement: Visual Analog Scale.;Level of agitation. Timepoint: 5, 10, and 20 minutes after arriving to recovery room, time to transfer from recovery to the ward, and also 1 and 6 hours after transfer to the ward. Method of measurement: Richmond Sedation Scale.

Secondary

MeasureTime frame
Opiom requirment. Timepoint: At recovery room and 6 hour after the surgery. Method of measurement: Submit file.;Patient hemodynamic. Timepoint: 5, 10, 20 minutes after the infusion and at exit the recovery room and 6 hour after the surgery. Method of measurement: Blood pressure and pulse rate (Monitoring instrument).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mahdi Saburi

Tehran University of Medical Sciences

Pouya.sabouri@gmail.com+98 21 63120

Outcome results

None listed

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