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Prediction of pain after surgery from pain due to venous cannulation and propofol infusion before surgery.

Prediction of postoperative pain from assessment of preoperative pain induced by venous cannulation and Propofol infusion

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/03/012616
Enrollment
93
Registered
2018-03-16
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: null- Patients undergoing elective laparoscopic cholecystectomy.

Interventions

None listed

Sponsors

Dr Yatish B
Lead Sponsor
Dr Yatish B
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients with American Society of Anaesthesiologists physical status I or II undergoing an elective laparoscopic cholecystectomy.

Exclusion criteria

Exclusion criteria: 1.Patient with history of recurrent preoperative pain 2.Inability to understand instructions 3.Contraindications to the study drugs

Design outcomes

Primary

MeasureTime frame
To determine the correlation between preoperative bedside VAS assessments of pain intensity associated with venous cannulation and propofol infusion and postoperative pain estimatesTimepoint: Postoperative pain intensity at rest,will be assessed from arrival in the post-anaesthesia care unit and at 10, 20, 30, 60 and 90 min in awake patients.—

Secondary

MeasureTime frame
The timing of first rescue dose of morphine and total dose of morphine at the end of 90 minutes.Timepoint: Measures of postoperative pain will be evaluated by pain intensity ratings, time from extubation to first dose of morphine, and total dose of morphine within 90 min.—

Countries

India

Contacts

Public ContactDr Pragya Mishra

Ramaiah Medical College and Hospitals

yatishseeni@yahoo.co.in9739388172

Outcome results

None listed

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