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Trial · NCT06243120

Intravenous Lidocaine for Treating Intrathecal Fentanyl Induced Pruritus

NCT06243120, Early phase 1, Unknown, Ain Shams University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Intravenous Lidocaine for Treating Intrathecal Fentanyl Induced Pruritus. Trials, record NCT06243120. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06243120

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Intravenous Lidocaine for Treating Intrathecal Fentanyl Induced Pruritus
NCT number
NCT06243120
Status
Unknown
Phases
Early phase 1
Enrollment
54 participants, estimated
Lead sponsor
Ain Shams University
Conditions
Pruritus Caused by Drug
Interventions
Lidocaine IV
First posted
2024-02-06
Last updated
2024-02-06

Source ClinicalTrials.gov

Registered outcomes4

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
Primaryregression of VAS in comparison to initial pruritus scale.The whole perioperative period
Before the surgery, patients could cooperate and understand the Visual Analogue Score (VAS) scale. The patients will be explained about the use of VAS for grading the severity of pruritus on a scale of 0 to 10. VAS = 0 means no pain or itching, VAS = 10 means worst sensation and VAS \> 4 means it needs intervention.
SecondaryThe percentage of incidence of pruritusThe whole perioperative periodobservation
Secondarybody distribution of pruritusThe whole perioperative periodobservation
Secondarylocal anesthetic toxicity symptoms.The whole perioperative periodobservation

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.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
25730811BACKGROUND

Source PubMed

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT06243120

GET https://conductscience.org/api/trials/v1/NCT06243120/registered