Clinical Trials Directory

Trials / Unknown

UnknownNCT02599623

Safety and Efficacy of Local Anesthesia in Emergency Inguinal Hernia Surgery

Safety and Efficacy of Local Anesthesia in Emergency Inguinal Hernia Surgery, a Prospective Randomized Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
RenJi Hospital · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

This prospective randomized is designed to evaluate the safety and efficacy of hernia repairs using local anesthesia compared with those using general anesthesia for patients with incarcerated hernia.

Detailed description

The outcome parameters measured included intraoperative conditions, postoperative conditions and long-term follow-up conditions.

Conditions

Interventions

TypeNameDescription
PROCEDURELocal AnesthesiaPatients in LA group received the local infiltration technique. A mixture of 2% lidocaine 20ml and 0.9%NS 30ml was used as the local anesthetic. Patients required extra analgesia during the surgery were given 20-40mg parecoxib sodium intravenously. Conversion to GA was performed if LA was intolerant for patient, which was evaluated by both anesthetists and surgeons.
PROCEDUREGeneral AnesthesiaIn group GA, anesthesia was induced with propofol 2mg/kg and fentanyl 0.1-0.2mg intravenously. Inhalation anesthesia was given at the same time with a mixture of oxygen and isoflurane 1-2% through an intubation.

Timeline

Start date
2016-01-01
Primary completion
2018-12-01
Completion
2019-12-01
First posted
2015-11-06
Last updated
2016-06-20

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02599623. Inclusion in this directory is not an endorsement.