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Early recovery from anaesthesia- A comparison between two common modes of anaesthesia: inhalational and total intravenous in short gynaecological surgeries

A comparison between inhalational and total intravenous anaesthesia in providing an early recovery in short gynaecological surgeries: A randomized controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094500
Enrollment
60
Registered
2025-09-10
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: PCS- Health Condition 2: O- Medical and Surgical Health Condition 3: N889- Noninflammatory disorder of cervixuteri, unspecified

Interventions

Intervention1: Total inhalational anaesthesia group: Patients will receive total inhalational anaesthesia with O2, N2O and sevoflurane Control Intervention1: Total intravenous anaesthesia group: Ptien

Sponsors

Amrita Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of the American Society of Anaesthesiologists (ASA) physical status 1?2, undergoing dilatation and curettage(D and C) procedures as ambulatory day case procedures under general anaesthesia will be included

Exclusion criteria

Exclusion criteria: Patients with known allergy to the drugs used will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
To compare the time taken to respond to verbal commands at the end of surgery between 2 groups of patientsTimepoint: 4 weeks

Secondary

MeasureTime frame
To compare the postoperative nausea and vomiting, surgeon and patient satisfactionTimepoint: At 1 hr post op

Countries

India

Contacts

Public ContactNitu PV

Amrita Institute of medical Sciences

aswinin99@gmail.com9446322702

Outcome results

None listed

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