FindTrial
Sign In

To evaluate the effect of intra-operative ketamine on incidence and severity of catheter related bladder discomfort in the post-operative period

Effect of intra-operative ketamine on post-operative Catheter Related Bladder Discomfort in abdominal surgeries: A Randomized Double Blind Interventional Controlled Study at S.M.S. Medical College and Attached Group of Hospitals, Jaipur during 2020-2021

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/01/030506
Enrollment
90
Registered
2021-01-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: K00-K95- Diseases of the digestive system

Interventions

Intervention1: INJECTION KETAMINE: Patients will receive 0.5mg/kg of ketamine diluted with normal saline to make a total volume of 2ml intravenously Control Intervention1: NORMAL SALINE: Patients will

Sponsors

Department of Anesthesiology Sawai Man Singh Medical College And Attached Hospitals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex. Age group between 20 years to 40 years. Weight between 50-80 Kg. ASA grade I & II. Undergoing abdominal surgery (Duration 60-120 min)

Exclusion criteria

Exclusion criteria: 1)Patients not willing to participate in the study. 2)History of urinary system obstruction that 3)needed surgical intervention. 4)History of neurological disorder, severe liver or heart disease. 5)History of overactive bladder ( urinating more than 3 times at night or 8 times during a 24-hour period). 6)History of chronic pain, opium abuse and morbid obesity. 7)If there was need for incision over supra- pubic area or bladder ,delayed extubation or a need for admission to the intensive care unit .

Design outcomes

Primary

MeasureTime frame
To determine the difference in percentage of cases who experience CRBD (catheter related bladder discomfort) during post-operative period in both groupsTimepoint: 6 Hours—

Secondary

MeasureTime frame
1) Mean duration of requirement of first rescue analgesia. 2) To determine the difference in percentage of cases who experience the side effects during the post-operative period in both groups. Timepoint: 6 Hours—

Countries

India

Contacts

Public ContactDr MAYURESH HANCHNAL

SMS Medical college,Jaipur.

bafnausha@yahoo.com9413901579

Outcome results

None listed

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