Comparative efficacy of high flow nasal cannula versus conventional oxygen delivery during procedural sedation for ovum pickup procedure

Comparative efficacy of high flow nasal cannula versus conventional oxygen delivery during procedural sedation for ovum pickup procedure - Nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/09/094158

Enrollment

220

Registered

2025-09-03

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: R37- Sexual dysfunction, unspecified Health Condition 2: 4- Measurement and Monitoring Health Condition 3: 4- Measurement and Monitoring

Interventions

Intervention1: Assisted ventilation if required when patient is desaturating: Assisted ventilation if required when patient is desaturating Intervention2: Comparison between HFNC and conventional oxyg

Eligibility

Inclusion criteria

Inclusion criteria: Female patients in ASA I and II Patients consenting to the study

Exclusion criteria

Exclusion criteria: ASA III IV Patients less than 18years Patients with cardiac illness Patients having COPD Emergency procedure BMI more than 30 Patients with OsA Patients anticipated with difficult airway Patients allergic to any drugs during sedation

Design outcomes

Primary

Measure	Time frame
To determine the incidence of desaturation events in High Flow Nasal Cannula (HFNC) group vs Conventional oxygen delivery group in all patients undergoing ovum pickup under procedural sedation.Timepoint: At T0,T1,T5,T10,T15,T20,T30	—

Secondary

Measure	Time frame
1. To evaluate & compare the need for assisted ventilation between the high flow nasal cannula group & conventional oxygen delivery group. 2. To calculate total propofol consumption in high flow nasal cannula group & conventional oxygen delivery group. 3. To assess clinician satisfaction on a 3-point satisfaction scale. 4. To assess patient satisfaction on a 5-point Likert scale. Timepoint: At T0,T1,T5,T10,T15,T20,T30	—

Measure

Time frame

1. To evaluate & compare the need for assisted ventilation between the high flow nasal cannula group & conventional oxygen delivery group. 2. To calculate total propofol consumption in high flow nasal cannula group & conventional oxygen delivery group. 3. To assess clinician satisfaction on a 3-point satisfaction scale. 4. To assess patient satisfaction on a 5-point Likert scale. Timepoint: At T0,T1,T5,T10,T15,T20,T30

—

Countries

India

Contacts

Public ContactVishal Mohan

Army hospital R and R

bhavnahooda2007@rediffmail.com9910663810

Outcome results

None listed

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