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Study on the application of intracervical block (Cervical injection)for painless hysteroscopy

Study on the application of intracervical block (Cervical injection)for painless hysteroscopy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123586
Enrollment
Unknown
Registered
2026-04-28
Start date
2026-05-06
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Hysteroscopy

Interventions

B Group:Intracervical block
N Group:Saline Injection

Sponsors

The First Affiliated Hospital of Qingdao University Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18–70 years; 2. ASA Class I–II; 3. Patients scheduled to undergo hysteroscopy under general anaesthesia without endotracheal intubation.

Exclusion criteria

Exclusion criteria: A. ASA=? B.Allergy to experimental drugs C. Combined with severe cardiac, pulmonary, hepatic, renal, neurological and psychiatric diseases D. Suffering from sleep apnea syndrome E.anemia or thrombocytopenia F.poor blood pressure control

Design outcomes

Primary

MeasureTime frame
Number of airway interventions;Hypoxiemia, SPO2 <95%;Propofol dosage;VAS;Hypotention SBP<90mmHg;Bradycardia;

Secondary

MeasureTime frame
Incidence of nausea and vomit;Incidence of fatigue;Incidence of dizzness;During of anesthesia;During of hysteroscopy;During of recovery;Satisfication level of patient;

Countries

China

Contacts

Public ContactLiu Shanling

The Affiliated Hospital of Qingdao University Medical College

lslsxmu@sina.com+86 178 5329 0630

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026