Postoperative Pain Management of Obese Patient Undergoing Gastric Bypass Surgery.

Title: Comparing The Effect Of Ketorolac and Morphine With Morphine Alone in Postoperative Pain Management of Obese Patient Undergoing Gastric Bypass Surgery.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20171014036769N2

Enrollment

Registered

2018-02-20

Start date

2017-12-22

Completion date

Unknown

Last updated

2018-03-26

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

Conditions

Condition 1: Post Operative Pain. Condition 2: Morbid Obesity. Other acute postprocedural pain Overweight and obesity

Interventions

Intervention 1: Intervention group: patients will receive PCA infusion of 0.4 mg morphine sulfate per hour and Apotel 1 gram intravenously every 12 hours plus 30 mg IV and 30 mg IM ketorolac and also

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Body Mass Index >40kg/m2 candidate for gastric bypass surgery Body mass Index > 35kg/m2 in addition to coexisting diseases such as diabetes, hypertension, renal disease, cardiovascular diseases ASA class : 1 or 2

Exclusion criteria

Exclusion criteria: reported Addiction to psychotropic drugs or substance abuse History of allergic reactions to drugs used in the study

Design outcomes

Primary

Measure	Time frame
VAS (Visual Analogue Scale) pain score. Timepoint: Immediately after the surgrey, 6 , 12 , 24 hours later and at the time of discharge. Method of measurement: Pain score questionnaire.	—

Secondary

Measure	Time frame
Post Operative Nausea and Vomiting. Timepoint: 0,6,12,24 hours after exiting recovery room. Method of measurement: questionnaire.;Length of Stay. Timepoint: at the time of discharge. Method of measurement: questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Soodeh Tabashi

Shahid Beheshti Medical University

school.of.medicine@sbmu.ac.ir+98 21 2387 2592

Outcome results

None listed

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