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Clinical research on medical suction systems and suction devices

Clinical research on medical suction systems and suction devices

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097396
Enrollment
Unknown
Registered
2025-02-19
Start date
2025-02-25
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

None

Interventions

Experimental group:Medical suction system suction device
Control group:Use the hospital's existing collection method for the liquid discharged after uterine cavity flushing, including disposable collection bags

Sponsors

Shaoxing People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Female patients aged 18-80 years old; 2) Patients who plan to undergo hysteroscopic surgery, indications include but are not limited to: myomectomy, endometrial polypectomy, suspected endometrial abnormalities, uterine space occupying lesions, abnormal uterine bleeding, uterine fluid accumulation, uterine adhesions, abnormal endometrial development, uterine septum, and other situations that require hysteroscopic resection surgery; 3) Patients with physical status grades I-II of the American Society of Anesthesiologists (ASA) ; 4) Patients or their families who understand and voluntarily sign informed consent forms.

Exclusion criteria

Exclusion criteria: 1) Patients with severe heart, lung, liver, and kidney dysfunction who cannot tolerate surgery; 2) Patients with coagulation dysfunction; 3) Pregnant or lactating women; 4) Patients with mental illness or those who are unable to cooperate with the study; 5) Patients participating in other clinical trials; 6) Patients with a history of water intoxication or hyponatremia; 7) Patients with preoperative abnormal blood sodium levels (145 mmol/L); 8) Patients who have used drugs that may affect fluid balance (such as diuretics, antidiuretic hormones, etc.) in the past 3 months; 9) Patients with severe endocrine disorders (such as thyroid dysfunction and adrenal dysfunction); 10) Patients with acute reproductive tract inflammation or cervical abnormalities; 11) According to the Clinical Practice Guidelines for Hysteroscopy Diagnosis and Surgery in China (2023 edition), contraindications for hysteroscopy surgery need to be included in the exclusion criteria. 12) The researchers believe that patients who are not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Accurate measurement of the inflow and outflow of uterine fluid;Water poisoning risk assessment;

Secondary

MeasureTime frame
The impact on surgical efficiency (waste liquid cleaning time);Hospital stay;Satisfaction of medical staff;Check the changes in data after using the equipment;

Countries

China

Contacts

Public ContactYungen Wang

Shaoxing People's Hospital

850981232@qq.com+86 135 8733 7050

Outcome results

None listed

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