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Trial · NCT04959799

Dalbavancin Real-life Utilization in Diabetic Patients Suffering From Infections (DALBADIA)

NCT04959799, Completed, Aziende Chimiche Riunite Angelini Francesco S.p.A

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Dalbavancin Real-life Utilization in Diabetic Patients Suffering From Infections (DALBADIA). Trials, record NCT04959799. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04959799

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Trial

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

Title
Dalbavancin Real-life Utilization in Diabetic Patients Suffering From Infections (DALBADIA)
NCT number
NCT04959799
Status
Completed
Enrollment
98 participants, actual
Lead sponsor
Aziende Chimiche Riunite Angelini Francesco S.p.A
Conditions
Diabetes, Infection
Interventions
Dalbavancin
First posted
2021-07-13
Last updated
2022-09-21

Source ClinicalTrials.gov

Registered outcomes7

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

ListOutcomeTime frameDescription
PrimaryRetrospective description of the dalbavancin treatment in diabetic patients.4 weeksEvidence of dalbavancin treatment choice (number and dates of infusions)
PrimaryRetrospective description of the utilization of dalbavancin treatment in diabetic patients.4 weeksEvidence of dalbavancin treatment choice (starting and subsequent dosage)
PrimaryRetrospective description of the setting of dalbavancin treatment in diabetic patients.4 weeksEvidence of dalbavancin treatment choice (setting of infusion)
SecondaryDemographic data4 weeksDemographic data description (Age and Gender)
SecondaryClinical cure of dalbavancinUp to 8 weeks
Number of patients with clinical cure evaluated by physicians at end of dalbavancin treatment (i.e., date of last dalbavancin dose administration). Clinical cure is defined as clinical signs and symptoms resolved.
SecondaryMicrobiological success of dalbavancinUp to 8 weeks
Number of patients with microbiological success at end of dalbavancin treatment (i.e., date of last dalbavancin dose administration). Microbioligical success is defined as culture-confirmed eradication of the Gram-positive pathogens identified at baseline, documented as a negative bacterial culture from the same site as the initial positive baseline culture
SecondaryIncidence of Adverse EventsUp to 8 weeksSafety profile was assessed through the incidence of Adverse Events occurred in patients treated with dalbavancin.

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
38211660DERIVED

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/NCT04959799

GET https://conductscience.org/api/trials/v1/NCT04959799/registered