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Application of Continuous Non-invasive Hemoglobin Monitoring in Assessing Fluid Tolerance in Patients Undergoing Hysteroscopic Surgery

Application of Continuous Non-invasive Hemoglobin Monitoring in Assessing Fluid Tolerance in Patients Undergoing Hysteroscopic Surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126346
Enrollment
Unknown
Registered
2026-06-08
Start date
2026-06-09
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Perioperative pulmonary edema during hysteroscopy

Interventions

Case series:None

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 60 years; 2. ASA physical status I–III; 3. Scheduled for elective hysteroscopic surgery with an expected duration of >30 minutes (e.g., hysteroscopic resection of submucosal myoma, adhesiolysis, septum resection, etc.); 4. Signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Severe cardiac, pulmonary, hepatic, or renal insufficiency; 2. Known arrhythmia or aortic valve regurgitation; 3. Anatomical abnormalities or history of surgery in the inferior vena cava (IVC) region; 4. Obesity (BMI >= 35 kg/m²) that compromises ultrasound image quality; 5. Emergency surgery or coagulation disorders.

Design outcomes

Primary

MeasureTime frame
hemoglobin concentration;

Secondary

MeasureTime frame
Pleth Variability Index;

Countries

China

Contacts

Public ContactXu Mao

Peking University Third Hospital

baolin23ad@163.com+86 10 8226 7260

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026