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Efficacy of crystalloid co-load for preventing hypotension in patients undergoing colonoscopy with intravenous propofol sedation

Efficacy of crystalloid co-load for preventing hypotension : randomized controlled trial

Status
Unknown
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240917003
Enrollment
154
Registered
2024-09-17
Start date
2024-09-03
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

intravenous propofol induced hypotension hypotension, colonoscope , sedate, coload, fluid

Interventions

fluid administration in maintenance dose ,Fluid loading(15ml/kg)in 30 minutes when start IV sedation
No Intervention No treatment,Experimental Drug
controlled group,coload

Sponsors

Faculty of medicine, Khon Kaen university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.age 18-65 years old 2.ASA PS 1-3 3.successful bowel preparations

Exclusion criteria

Exclusion criteria: 1.colonoscope with EGD 2.Cardiovascular disease (CHF, MI, low LVEF < 50%) 3.ESRD (eGFR<30ml/min) 4.Poorly controlled DM 5.Obesity BMI > 35 6.Serum albumin < 3 mg/dL 7.IPD case whom received fluid before waiting area

Design outcomes

Primary

MeasureTime frame
Hypotension 24 hours postoperatively Automatic arm blood pressure monitor—

Secondary

MeasureTime frame
complication of hypotension ; volume overload,MI intraoperative and 24 hours postoperative review clinical in IPD case and telephone visit in OPD case—

Countries

Thailand

Contacts

Public ContactChonthisa Kongsarai

Faculty of Medicine, Khon Kaen University

chonko@kku.ac.th0909710187

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026