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Effect of crystal preloading on hypotension during propofol sedation for gastroenteroscopy

The observation and study of hypotension during propofol sedation for gastroenteroscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082021
Enrollment
Unknown
Registered
2024-03-19
Start date
2024-04-15
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

Population undergoing propofol sedation for gastroenteroscopy

Interventions

Control Group :N/A
Experimental Group :Intravenous 10 ml/kg Ringer's lactate solution for preloading

Sponsors

Wuxi People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: ? ASA I-II, Mallampati grade 1-2; ? Blood pressure was well controlled in patients with hypertension below grade 1; ? Without serious cardiovascular diseases; ? No history of chronic liver and kidney diseases; ? Body Mass Index (BMI)< 30; ? Preoperative evaluation showed no risk of difficult airway or sleep apnea syndrome ? No definite chronic intestinal disease ? No history of allergy to anesthetic drugs.

Exclusion criteria

Exclusion criteria: Exclusion criteria: (1) Examination time more than 30 minutes; ? Active chronic intestinal diseases; ? Suspected allergic patients.

Design outcomes

Primary

MeasureTime frame
SBP;MAP;—

Secondary

MeasureTime frame
HR;SpO2;Awakening time;Duration of examination;Total amount of propofol;Ephedrine dosage;—

Countries

China

Contacts

Public ContactGuilong Wang

Wuxi People’s Hospital

guilwang@aliyun.com+86 137 7100 5107

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026