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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Local Anesthesia | Patients 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. |
| PROCEDURE | General Anesthesia | In 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.