At a glance
ClinicalIndex Comparison RecordN/ACompleted· 48 enrolled
Drug / intervention
Propofol +4 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
the Safety and Effectiveness of the Effects on the Perioperative Pain Control Comparing Between the Thoracic Paravertebral Nerve Block Using the Camera Guided and the Intrathoracic Intercostals Nerve Block for the Management of Nonintubated Local Regional Analgesia in Uniport Thoracoscopic Surgery for the Undetermined Solitary Nodules Patients
In Brief
A clinical study evaluating Propofol, Sulfentanyl, and 3 other interventions for Peripheral Solitary Pulmonary Nodule or Tuberculoma. Completed, enrolled 48 participants across 1 site.
Detailed Summary
The aim of this study is to study the safety and effectiveness of the effects on the perioperative pain control comparing between the thoracic paravertebral nerve block using the camera guided and the intrathoracic intercostals nerve block for the management of nonintubated local regional analgesia in uniport thoracoscopic surgery for the undetermined solitary nodules patients.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--
Timeline
N/ACompletedFinished
2017201820192020202120222023202420252026
Enrollment StartMar 2017
First PostedMar 2017
Primary CompletionSep 2019
Study CompletionSep 2019
TodayJul 2026
First PostedMar 22, 2017
Enrollment StartMar 1, 2017
Primary CompletionSep 1, 2019
Study CompletionSep 5, 2019
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 9.3 years ago
Interventions
Propofoldrug
anaesthetic
Sulfentanyldrug
anaesthetic
Dexmedetomidinedrug
anaesthetic
Lidocainedrug
local anaesthetics
Ropivacainedrug
local anaesthetics