A multicenter randomized controlled study comparing blunt needle suture and sharp needle suture in preventing transdermal exposure during obstetric surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100050979

Enrollment

Unknown

Registered

2021-09-09

Start date

2021-10-01

Completion date

Unknown

Last updated

2022-05-16

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

Conditions

None listed

Interventions

Experimental group:blunt needle suture

Control group:sharp needle sutures

Eligibility

Sex/Gender

Female

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Parturients who undergo cesarean section, episiotomy or perineal laceration during childbirth and need to implement soft tissue suture; 2. Voluntarily participate in this study and sign informed consent; 3. The surgeons have completed at least 100 surgeries related to their specialty.

Exclusion criteria

Exclusion criteria: 1. Deaf in both ears, blindness in both eyes; 2. Inability to communicate effectively.

Design outcomes

Primary

Measure	Time frame
Incidence of needlestick injuries caused by medical staff sutures;Operation time;Intraoperative blood loss;Needle ease of use score;Adverse event rate;Total cost of hospitalization;Total cost of surgery;Hospital stay;	—

Countries

China

Contacts

Public ContactLiu Ting

Xuanwu Hospital Capital Medical University

tingting9718@126.com+86 13701289718

Outcome results