A study to determine the best fluid therapy during surgery for patients undergoing gynecological surgeries

Liberal versus Restrictive Fluid Management in Ambulatory Laparoscopic Gynaecological Surgeries: A Randomized Controlled Trial - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/11/097138

Enrollment

Registered

2025-11-10

Start date

Unknown

Completion date

Unknown

Last updated

2025-11-17

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

Conditions

Health Condition 1: N849- Polyp of female genital tract, unspecified Health Condition 2: N709- Salpingitis and oophoritis, unspecified Health Condition 3: N719- Inflammatory disease of uterus, unspecified Health Condition 4: N74- Female pelvic inflammatory disorders in diseases classified elsewhere Health Condition 5: N809- Endometriosis, unspecified Health Condition 6: N839- Noninflammatory disorder of ovary,fallopian tube and broad ligament, unspecified

Interventions

Intervention1: Intraoperative Libral Fluid Management: Intraoperative Libral fluid administration (40ml/kg) for 1 hour followed by 2ml/kg for the remaining intraoperative period Intervention2: Intraop

Eligibility

Inclusion criteria

Inclusion criteria: 1 ASA I-II 2 Duration of surgery less than 90 minutes 3 Diagnostic laparoscopy and hysteroscopy 4 Minor laparoscopic procedure

Exclusion criteria

Exclusion criteria: 1 Patient refusal 2 Hemoglobin level less than 10gm percent 3 Known cardiac or renal disease

Design outcomes

Primary

Measure	Time frame
Time to attain hospital discharge criteriaTimepoint: Time in minutes from arrival in PACU to discharge readiness with Modified PADDS score of 9 or more	—

Secondary

Measure	Time frame
Postoperative painTimepoint: Pain using Visual Analogue Scale of 100 mm on arrival at PACU and at Discharge;Postoperative Nausea and Vomiting PONVTimepoint: PONV score using a 0 to 3 PONV score on arrival in PACU and at discharge;Presence or absence of dizziness fatigue and thirstTimepoint: Recorded as binary response Yes/No on arrival in PACU and at Discharge;Modified PADSS score for discharge readinessTimepoint: On Arrival in PACU and At Discharge	—

Measure

Time frame

Postoperative painTimepoint: Pain using Visual Analogue Scale of 100 mm on arrival at PACU and at Discharge;Postoperative Nausea and Vomiting PONVTimepoint: PONV score using a 0 to 3 PONV score on arrival in PACU and at discharge;Presence or absence of dizziness fatigue and thirstTimepoint: Recorded as binary response Yes/No on arrival in PACU and at Discharge;Modified PADSS score for discharge readinessTimepoint: On Arrival in PACU and At Discharge

—

Countries

India

Contacts

Public ContactDR RAM SINGH

All India Institute of Medical Sciences New Delhi

dr.ram2001@gmail.com9958311829

Outcome results

None listed

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