Trial · NCT05348278
Urea Cream Prevention for Capecitabine Associated Hand Foot Syndrome
NCT05348278, Phase 2, Phase 3, Unknown, Mahidol University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Urea Cream Prevention for Capecitabine Associated Hand Foot Syndrome. Trials, record NCT05348278. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05348278
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Urea Cream Prevention for Capecitabine Associated Hand Foot Syndrome
- NCT number
- NCT05348278
- Status
- Unknown
- Phases
- Phase 2, Phase 3
- Enrollment
- 214 participants, estimated
- Lead sponsor
- Mahidol University
- Conditions
- Hand-Foot Syndrome
- Interventions
- Urea cream
- First posted
- 2022-04-27
- Last updated
- 2022-04-27
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | any HFS | from starting capecitabine until 4 week after capecitabine discontinuation | incidence of any HFS |
| Secondary | severe HFS | from starting capecitabine until 4 week after capecitabine discontinuation | grade 3 or 4 HFS |
| Secondary | time to develop severe HFS | from starting capecitabine until 4 week after capecitabine discontinuation | time for starting capecitabine to time of \>grade II HFS reported |
| Secondary | capecitabine interruption | from starting capecitabine until 4 week after capecitabine discontinuation | proportion of patient with capecitabine interruption due to HFS |
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.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 39962445 | DERIVED |
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.
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/NCT05348278
GET https://conductscience.org/api/trials/v1/NCT05348278/registered