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Trial · NCT03769298

CIRTEN-Simultaneous Pancreas-Kidney Transplant Recipients

NCT03769298, Phase 2, Phase 3, Recruiting, University of Wisconsin, Madison

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. CIRTEN-Simultaneous Pancreas-Kidney Transplant Recipients. Trials, record NCT03769298. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03769298

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Trial

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

Title
CIRTEN-Simultaneous Pancreas-Kidney Transplant Recipients
NCT number
NCT03769298
Status
Recruiting
Phases
Phase 2, Phase 3
Enrollment
20 participants, estimated
Lead sponsor
University of Wisconsin, Madison
Conditions
Kidney Pancreas Transplantation
Interventions
Envarsus XR
First posted
2018-12-07
Last updated
2026-10-29

Source ClinicalTrials.gov

Registered outcomes10

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

ListOutcomeTime frameDescription
PrimaryChange in patient and physician-assessed degree of tremors based on Fahn-Tolosa-Marin Tremor Rating ScaleOver 6 monthsFTM-TRS will be used as a tool for essential tremor scoring. (0: no tremor, 1: barely perceptible tremor, 2: \< 2 cm, 3: 2-4 cm, and 4: \> 4 cm).
PrimaryChange in patient and physician-assessed degree of tremors based on Quality of Life in Essential Tremor (QUEST) QuestionnaireOver 6 months
QUEST Questionnaire, a scoring tool will be used to measure the quality of life among patients with Essential Tremor. It consists of 30 items which are rated on a five-point scale (score 0-4), corresponding to the frequency (never, rarely, sometimes, frequently, always) with which tremor was perceived to affect a function or to be associated with various feelings and attitudes. A few items (e.g. 'I had to quit my job because of tremor') could only be answered at the extremes (yes/no; true/false), and these were scored either 0 or 4.
PrimaryScores on Quality of Life in Essential Tremor QuestionnairesOver 6 monthsUse QUEST (Quality of Life in Essential Tremor Questionnaire) scoring tool
PrimaryScores on Modified Transplant Symptom Occurrence and Symptom Distress Scale (MTSOSD) QuestionnaireOver 6 monthsMTSOSD Questionnaire scores will be used to assess the presence and distress of side effects associated with the use of immunosuppressive drugs after transplantation.
SecondaryRenal function by eGFR (estimated Glomerular Filtration Rate)Over 6 monthsChange between baseline and post-conversion as measured by eGFR
SecondaryRenal function by serum creatinineOver 6 monthsChange between baseline and post-conversion as measured by serum creatinine
SecondaryComparable or improved glycemic control as measured by mixed meal tolerance testOver 6 monthsChange between baseline and post-conversion
SecondaryComparable or improved glycemic control as measured by HbA1cOver 6 monthsChange between baseline and post-conversion
SecondaryTacrolimus doses and levelsOver 6 monthsChange between baseline and post-conversion
SecondaryMycophenolate doses and levelsOver 6 monthsChange between baseline and post-conversion

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.

Papers7

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
17343274BACKGROUNDPubMed
23339473BACKGROUNDPubMed
25593845BACKGROUNDPubMed
26113208BACKGROUNDPubMed
27017888BACKGROUNDPubMed
27109969BACKGROUNDPubMed
29241340BACKGROUNDPubMed

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/NCT03769298

GET https://conductscience.org/api/trials/v1/NCT03769298/registered