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Thoracic Paravertebral Blocks Using a Combination of Ropivacaine and Dexmedetomidine

Thoracic Paravertebral Blocks Using a Combination of Ropivacaine and Dexmedetomidine

Status
Withdrawn
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03677115
Enrollment
0
Registered
2018-09-19
Start date
2018-11-01
Completion date
2023-03-30
Last updated
2021-11-12

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

Conditions

Thoracic Paravertebral Blocks

Brief summary

The investigators designed a study to assess whether thoracic paravertebral blocks using a combination of ropivacaine and dexmedetomidine prolong nerve block duration.

Detailed description

The investigators designed a study to assess whether thoracic paravertebral blocks using a combination of ropivacaine and dexmedetomidine prolong nerve block duration. The effects of dexmedetomidine have only been compared at lower doses. This trial examined the effect of greater dose of dexmedetomidine on thoracic paravertebral block analgesia duration.

Interventions

DRUGDexmedetomidine

combination of ropivacaine and dexmedetomidine 20 ug every time

Sponsors

China Medical University, China
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

a single-dose thoracic paravertebral analgesia for postoperative pain control after thoracoscopic lobectomy

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients were included in the study if they were ethnic Chinese, * American Society of Anesthesiologists (ASA) physical status I or II, * candidates for general anesthesia undergoing thoracic surgery

Exclusion criteria

* Patients were excluded if they do not want to cooperate with the test, * had a history of radial artery puncture or coronary artery bypass grafting, * had acute vessel trauma,or had been diagnosed with Raynaud' disease, * had suffered from mental or neurological disorders

Design outcomes

Primary

MeasureTime frameDescription
Change of analgesia durationChange from Baseline to 3 days after surgeryChange of thoracic paravertebral block analgesia duration

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026