Trial · NCT06214169
Effect of Addition of Cisatracurium to Lidocaine VS Plain Lidocaine
NCT06214169, Not applicable, Completed, Watim Medical & Dental College
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effect of Addition of Cisatracurium to Lidocaine VS Plain Lidocaine. Trials, record NCT06214169. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06214169
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effect of Addition of Cisatracurium to Lidocaine VS Plain Lidocaine
- NCT number
- NCT06214169
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 44 participants, actual
- Lead sponsor
- Watim Medical & Dental College
- Conditions
- Anesthesia
- Interventions
- Cisatracurium Besylate, Lignocaine
- First posted
- 2024-01-19
- Last updated
- 2024-01-19
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time to onset of Sensory blockade. | 1-5 min. | Sensory block will be assessed by pinprick in the dermatomal sensory distribution and time noted for complete sensory blockade. |
| Primary | Time to onset of Motor Blockade | 2-7 min. | Motor block will be assessed by asking the subject to flex and extend his/her wrist and fingers, every 30 seconds and time to be noted till inability to flex or extend the wrist and fingers is confirmed and time noted. |
| Primary | Intraoperative Pain Scoring | 5-45 min. | The severity of intraoperative pain will be assessed using 10 point VAS (Visual Analogue Score) with 1 being no pain and 10 being the worst possible pain at 5, 10, 20, 30 minutes after tourniquet application. |
| Primary | Regression of sensory blockade | 2-10 min post deflation. | Sensory blockade regression time (the time elapsed from tourniquet deflation to recovery of complete sensation in all dermatomes, determined by pinprick test) , will be noted. |
| Primary | Regression of motor blockade | 2-10 min post deflation | Motor block regression time (the time elapsed from tourniquet deflation until regaining of flexion and extension of wrist and fingers) will be noted. |
| Primary | Postop Pain scoring | 5 minutes post deflaton till 8 hours post deflation. | Postoperative pain will be assessed by VAS at 5 minutes after tourniquet deflation and at 1, 2, 4, 8 hours postoperatively. |
| Primary | Time to first analgesic request post operatively. | 1 hour - 8 hours post deflation. | The first analgesic dose requirement time will also be noted (the time elapsed from tourniquet release until first request for analgesic medication postoperatively) |
| Primary | Side Effects | From onset of blockade to 8 hours post operatively. | Incidence of side effects such as tinnitus, dizziness, convulsions, gastric discomfort, muscle weakness and bleeding tendency will be recorded intraoperatively as well as during recovery from blockade. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers3
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT06214169
GET https://conductscience.org/api/trials/v1/NCT06214169/registered