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Safety and efficacy of preoperative 1h oral clear fluids in adults with cardiac patients: A randomized controlled trial

Safety and efficacy of preoperative 1h oral clear fluids in adults with cardiac patients: A randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17011112
Enrollment
Unknown
Registered
2017-04-11
Start date
2017-04-13
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

cardiac disease

Interventions

Experimental versus control:preoperative 1h oral clear fluids

Sponsors

The Union Hospital of Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. aged 18-65 years old; 2. ASA physical status I or II; 3. prepare for cardiac; 4. operation willing to join this study.

Exclusion criteria

Exclusion criteria: 1. definitive diagnosis of digestive syndrome; 2. severe complications of main organs such as liver, kidney; 3. regularly take the digestive medicine recently; 4. Mental retardation

Design outcomes

Primary

MeasureTime frame
State-Trait?Anxiety?Inventory;gastric residual;PH of gastric residual;vomiting and aspiration;heart rate;thirst;—

Countries

China

Contacts

Public ContactYanjuan Lin

The Union Hospital of Fujian Medical University

fjxhlyj@163.com+86 13365910562

Outcome results

None listed

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