Trial · NCT06376058
Chloroprocaine 1% Versus Ropivacaine 0,75% During Cesarean Section
NCT06376058, Not applicable, Recruiting, Aretaieion University Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Chloroprocaine 1% Versus Ropivacaine 0,75% During Cesarean Section. Trials, record NCT06376058. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06376058
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Chloroprocaine 1% Versus Ropivacaine 0,75% During Cesarean Section
- NCT number
- NCT06376058
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 60 participants, estimated
- Lead sponsor
- Aretaieion University Hospital
- Conditions
- Cesarean Section, Local Anesthetic
- Interventions
- Chloroprocaine 1% Injectable Solution, Ropivacaine 0.75% Injectable Solution
- First posted
- 2024-04-19
- Last updated
- 2025-07-22
Source ClinicalTrials.gov
Registered outcomes39
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time from spinal anesthesia to T10 block (min) | intraoperative | time required from spinal anesthetic injection to anesthetic block up to the 10th thoracic neurotome |
| Primary | Time from spinal anesthesia to T4 block (min) | intraoperative | time required from spinal anesthetic injection to anesthetic block up to the 4th thoracic neurotome |
| Primary | Time of spinal anesthesia to Bromage =3 | intraoperative | time required from spinal anesthetic injection to complete motor block (Bromage scale=3, where Bromage=0, no block; Bromage=1, partial block; Bromage=2, almost complete block; Bromage=3, complete block |
| Primary | level of sensory block every 3 min | intraoperative | measurement of sensory block every 3 minutes after spinal anesthesia during the first 15 minutes |
| Primary | level of sensory block every 15 min | intraoperative | measurement of sensory block every 15 minutes from spinal anesthesia to the end of the surgery |
| Primary | highest level of sensory block | intraoperative | measurement of the highest level of sensory block after intrathecal infusion of local anesthetic |
| Primary | time from spinal anesthesia to highest level of sensory block | intraoperative | time from the performance of spinal anesthesia to the highest level of sensory block |
| Primary | duration of sensory block | intraoperative | measurement of time required for the sensory block to regress from sensory level T4 to sensory level T12/L2 |
| Primary | pain at surgical incision | intraoperative | pain at skin incision using Visual Analogue Scale (VAS), where VAS=0, no pain; VAS=10, worst pain imaginable |
| Primary | pain at neonatal delivery | intraoperative | pain at neonatal delivery using VAS scale, where VAS=0, no pain; VAS=10, worst pain imaginable |
1 to 10 of 39Source ClinicalTrials.gov
See all 39 registered outcomesOutcomes0
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.
Papers4
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/NCT06376058
GET https://conductscience.org/api/trials/v1/NCT06376058/registered?page=2