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Trial · NCT03880578

Quality of Life After Interventional Thyroid Treatment

NCT03880578, Completed, Klinikum Lüdenscheid; results first posted 2024-10-29

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Quality of Life After Interventional Thyroid Treatment. Trials, record NCT03880578. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03880578

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Trial

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

Title
Quality of Life After Interventional Thyroid Treatment
NCT number
NCT03880578
Status
Completed
Enrollment
101 participants, actual
Lead sponsor
Klinikum Lüdenscheid
Conditions
Thyroid; Deficiency, Quality of Life
Interventions
Levothyroxine Sodium
First posted
2019-03-19
Last updated
2024-10-29
Results first posted
2024-10-29

Source ClinicalTrials.gov

Registered outcomes5

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

ListOutcomeTime frameDescription
PrimaryThyPRO Scale Scores (0-100, Higher Scores Indicating Worse Quality of Life)6 monthsquality of life measured by a thyroid specific validated questionnaire
SecondaryRate of Global Deiodinase Activity (SPINA-GD, See Reference Calculated Parameters)6 monthsefficiency of converting T4 into T3
OtherSerum Concentration of TSH6 monthsTSH
OtherSerum Concentrations of FT3 and FT46 monthsThyroid hormones FT3, FT4
OtherThyroid Volume Measured by Ultrasound (ml)6 monthsthyroid capacity

Outcomes5

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYThyPRO Scale Scores (0-100, Higher Scores Indicating Worse Quality of Life)6 monthsscoreMEAN
SECONDARYRate of Global Deiodinase Activity (SPINA-GD, See Reference Calculated Parameters)6 monthsnmol/sMEAN
OTHER_PRE_SPECIFIEDSerum Concentration of TSH6 monthsmIU/LMEAN
OTHER_PRE_SPECIFIEDSerum Concentrations of FT3 and FT46 monthspmol/LMEAN
OTHER_PRE_SPECIFIEDThyroid Volume Measured by Ultrasound (ml)6 monthsmlMEAN

Results by group12

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
ThyPRO Scale Scores (0-100, Higher Scores Indicating Worse Quality of Life)Control18.3Standard Deviation 10.8score
ThyPRO Scale Scores (0-100, Higher Scores Indicating Worse Quality of Life)Radioiodine19.9Standard Deviation 14.8score
Rate of Global Deiodinase Activity (SPINA-GD, See Reference Calculated Parameters)Control32.9Standard Deviation 5.03nmol/s
Rate of Global Deiodinase Activity (SPINA-GD, See Reference Calculated Parameters)Radioiodine32.2Standard Deviation 5.52nmol/s
Serum Concentration of TSHControl1.39Standard Deviation 0.63mIU/L
Serum Concentration of TSHRadioiodine2.34Standard Deviation 2.58mIU/L
Serum Concentrations of FT3 and FT4ControlFT35.33Standard Deviation 0.60pmol/L
Serum Concentrations of FT3 and FT4RadioiodineFT34.84Standard Deviation 0.65pmol/L
Serum Concentrations of FT3 and FT4ControlFT415.2Standard Deviation 2.13pmol/L
Serum Concentrations of FT3 and FT4RadioiodineFT414.2Standard Deviation 2.38pmol/L

Participant flow12

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDSurgery (Withdrawn, Not Continuing Recruiting)0
Overall StudySTARTEDRadioiodine51
Overall StudySTARTEDControl50
Overall Study12 MonthsSurgery (Withdrawn, Not Continuing Recruiting)0
Overall Study12 MonthsRadioiodine14
Overall Study12 MonthsControl19
Overall StudyCOMPLETEDSurgery (Withdrawn, Not Continuing Recruiting)0
Overall StudyCOMPLETEDRadioiodine47
Overall StudyCOMPLETEDControl49
Overall StudyNOT COMPLETEDSurgery (Withdrawn, Not Continuing Recruiting)0

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 totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityControl050
Total, all-cause mortalityRadioiodine151
Total, other adverse eventsControl050
Total, other adverse eventsRadioiodine051
Total, serious adverse eventsControl050
Total, serious adverse eventsRadioiodine051

Papers9

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
23184912BACKGROUNDPubMed
26335522BACKGROUNDPubMed
26635726BACKGROUNDPubMed
27257805BACKGROUNDPubMed
27375554BACKGROUNDPubMed
29155897BACKGROUNDPubMed
29375474BACKGROUNDPubMed
29396968BACKGROUNDPubMed
30022470BACKGROUNDPubMed

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 comparisons2

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
Radioiodine vs Control: deaths from any causeTrial comparisons
Radioiodine vs Control: serious adverse eventsTrial comparisons

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/NCT03880578

GET https://conductscience.org/api/trials/v1/NCT03880578/registered