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A study to compare intravenous paracetamol and intravenous paracetamol with dexmedetomidine for pain relief after gynaecological surgeries

A comparison of intravenous paracetamol and intravenous paracetamol with dexmedetomidine for post operative analgesic management in gynaecological surgeries - A randomised double blinded study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/02/023178
Enrollment
70
Registered
2020-02-07
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: N80-N98- Noninflammatory disorders of female genital tract

Interventions

Intervention1: Paracetamol: Ten minutes before the completion of the procedure, Paracetamol given in intravenous route of dose 0.5 - 1 gram over 10 minutes Intervention2: Paracetamol with Dexmedetomid

Sponsors

Srinithi A
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing elective gynaecological surgeries Patients categorised under American Society of Anaesthesiologist I or II

Exclusion criteria

Exclusion criteria: History of allergy to Paracetamol, Dexmedetomidine BMI 30 Patients categorised under American Society of Anaesthesiologist III and above Patients with coagulopathy

Design outcomes

Primary

MeasureTime frame
To compare the post operative pain score between intravenous Paracetamol and intravenous paracetamol with dexmedetomidineTimepoint: Postoperative Period—

Secondary

MeasureTime frame
To compare the time for the first analgesic requirement after surgery To assess the hemodynamic changes To assess the sedation score To compare the opioid consumptionTimepoint: Postoperative Period—

Countries

India

Contacts

Public ContactSrinithi A

Shri sathya sai medical college and research institite

Esenkeyem@gmail.com9786743120

Outcome results

None listed

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