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Comparison of sedative medication to non-sedative medication for pain relief during and after laproscopic surgery

Comparison of the effect of Non-opioid adjuvants with opioid adjuvants for peri-operative analgesia and recovery from anaesthesia in laproscopic surgeries- A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/08/027401
Enrollment
88
Registered
2020-08-26
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: O- Medical and Surgical

Interventions

Intervention1: Intravenous fentanyl infusion for peri-operative analgesia: in one group intravenous fentanyl infusion along with lignocain intravenous infusion will be given and peri-operative analges

Sponsors

Pramukhswami medical College Shree Krishna Hospital Bhaikaka University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients aged 18 to 60 years who can give informed consent and posted for laproscopic surgeries who belong to American society of anaesthesiologist physical status grade 1 to 3 are included for the study.

Exclusion criteria

Exclusion criteria: ASA grade 4 and 5 patients, patients with hepatic,cardiac renal insufficiency, Body mass index >40,pregnant and breast feed patients,patients with conduction defect and basal heart rate <50 beats per minute and patients with psychiatric illness, intracranial pathology and who are not willing to give consent are excluded from the study.

Design outcomes

Primary

MeasureTime frame
Study of post operative pain relief using visual analogue scoreTimepoint: Study of post operative pain relief using visual analogue scoreimmediate after surgery and at the interval of 1hour 2 hour 4 hr 8hr 12 hr till 24 hours.

Secondary

MeasureTime frame
Ambulation trial of patient after surgery will be monitored.Timepoint: Time of ambulation after surgery will be noted.;incidence of post operative nausea vomitting .Timepoint: Time of post operative nausea vomitting will be noted.;Passage of flatus and or stool will be monitored.Timepoint: Time of passage of stool and or flatus after surgery will be noted.;Requirement of rescue analgesia.Timepoint: Time of rescue analgesia and name and dose of medication will be noted

Countries

India

Contacts

Public ContactDr Bhumika Pathak

Pramukhswami Medical College

docbhum29@yahoo.com9904438877

Outcome results

None listed

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