Effect of ropivacaine with different specific gravity on cervical cerclage

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2300068386

Enrollment

Unknown

Registered

2023-02-16

Start date

2023-02-20

Completion date

Unknown

Last updated

2023-05-22

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

Conditions

cervical incompetence

Interventions

Observation group:Hypobaric ropivacaine

control group: isobaric ropivacaine

Eligibility

Sex/Gender

Female

Age

25 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1: Elective operation 2: 25-35 years old 3: 14-28weeks gestation 4: ASA?~?

Exclusion criteria

Exclusion criteria: 1: Severe early pregnancy reaction 2: Patients with severe comorbidities before surgery 3: Patients with contraindications to intraspinal anesthesia 4: Mental and intellectual problems, unable to cooperate with researchers

Design outcomes

Primary

Measure	Time frame
Incidence of supine hypotension;	—

Secondary

Measure	Time frame
Onset time of anesthesia;Anesthesia block plane;Duration of motor block;Pain score;Incidence of nausea and vomiting;Use of vasoactive drugs;Satisfaction of patients and doctors;	—

Countries

China

Contacts

Public ContactLiyan Miao

Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University

384446787@qq.com18396129126

Outcome results

None listed

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