Skip to content

COMPARATIVE STUDY OF USG guided QUALITATIVE AND QUANTITATIVE ASSESSMENT OF GASTRIC VOLUME PRE-OPERATIVELY IN FULL TERM PREGNANT FEMALES V/S NONPREGNANT PATIENTS POSTED FOR ELECTIVE SURGERIES.

COMPARATIVE STUDY OF QUALITATIVE AND QUANTITATIVE ASSESSMENT OF GASTRIC VOLUME PRE-OPERATIVELY IN FULL TERM PREGNANT FEMALES V/S NONPREGNANT PATIENTS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2022/06/043329
Enrollment
140
Registered
2022-06-17
Start date
Unknown
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Health Condition 1: O740- Aspiration pneumonitis due to anesthesia during labor and delivery Health Condition 2: R198- Other specified symptoms and signsinvolving the digestive system and abdomen

Interventions

Control Intervention1: Not applicable: Not applicable Control Intervention2: Usg guided observation of gastric volume pre operatively: Comparing pregnant females with non pregnant female patients post

Sponsors

Department of anaesthesiology Saveetha medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 2 nd 3 , full term pregnant females and non pregnant female patients posted for other elective surgeries.

Exclusion criteria

Exclusion criteria: ï?? ASA score 3, 4. ï?? Multiple gestations. ï?? pre-existing abnormal anatomy of the upper gastrointestinal tract (previous lower oesophageal or gastric surgery, hiatal hernia, and gastric cancer). ï?? Patient refusal to consent

Design outcomes

Primary

MeasureTime frame
To compare qualitative and quantitative assessment og gastric volume pre operatively in full term pregnant females versus non pregnant female patients. Timepoint: Outcome analyses will be done from 16 to 20 weeks

Secondary

MeasureTime frame
Compare standard fasting guidelines and usg assements of gastric volumeTimepoint: Will be analysed and compared at 16 to 20 weeks after the start of study

Countries

India

Contacts

Public ContactMouriya S

Saveetha medical college

nikiladg@gmail.com9535243669

Outcome results

None listed

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