Trials / Unknown
UnknownNCT04763434
Dexamethasone and Dexmedetomidine as Adjuvants to Ropivacaine in Ultrasound-guided Multilevel Thoracic Paravertebral Block for Lobectomy: A Prospective, Randomized, Triple-blind Study
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 90 (estimated)
- Sponsor
- Gansu Provincial Hospital · Academic / Other
- Sex
- All
- Age
- 16 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The hypothesis is whether perineural dexamethasone and dexmedetomidine prolonged the duration of analgesia as compared with either perineural dexamethasone or perineural dexmedetomidine after TPVB.
Detailed description
Design: A prospective, randomized, controlled study Setting: Single-center university hospital. Participants: The study included 90 patients undergoing lobectomy under general anesthesia. Interventions: The patients were allocated randomly into the following 3 groups: 20 ml mixture of 37.5 mg ropivacaine with 5 mg dexamethasone (RS group) or 1 µg/kg dexmedetomidine (RM group), or with 1 µg/kg dexmedetomidine and 5 mg dexamethasone (RSM group). Ultrasound-guided TPVB was performed at 4 points-T4-5, T5-6, T6-7, and T7-8 of the surgical side; 5 mL of solution were injected at each point. Postoperatively, the PCIA was used as part of multimodal analgesia, and all patients recieve .
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | dexamethasone; dexmedetomidine; ropivacaine | Ultrasound-guided multilevelTPVB is performed at the end of lobectomy |
Timeline
- Start date
- 2021-03-20
- Primary completion
- 2021-08-20
- Completion
- 2021-08-30
- First posted
- 2021-02-21
- Last updated
- 2021-02-21
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT04763434. Inclusion in this directory is not an endorsement.