Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04431960 · ClinicalTrials.gov registry record · Phase 1

Blackcurrants Modify Gut Microbiota and Reduce Osteoporosis and CVD Risk

A Phase 1 study, sponsored by University of Connecticut.

Completed
Registry status
Phase 1
Development phase
51
Enrollment target

NCT04431960: Completed Phase 1 study, sponsored by University of Connecticut.

NCT04431960 is a Phase 1 study that has completed, run by University of Connecticut. The registered enrollment target is 51 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (15% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04431960, a Phase 1 study, has completed, sponsored by University of Connecticut.

COMPLETED
Registry status
Phase 1
Development phase
51 participants
Enrollment target

Study Summary

Aim to evaluate the effects of blackcurrant supplementation on changes in gut microbiome, bone mass, and CVD risk factors in adult women.

Primary Outcome

Changes in BMD of whole-body measured via dual energy x-ray absorptiometry

Interventions

  • DRUG blackcurrant (BC) extract

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2021-07-20
Est. Completion 2022-10-03
Phase Phase 1
University of Connecticut

107 total trials

What the finished NCT04431960 record still lists

NCT04431960 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 51 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (15% lower).

The record links to 0 conditions, and to 1 intervention - of which blackcurrant (BC) extract is the first listed.

NCT04431960 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04431960 about?

NCT04431960 is a clinical study titled "Blackcurrants Modify Gut Microbiota and Reduce Osteoporosis and CVD Risk". Aim to evaluate the effects of blackcurrant supplementation on changes in gut microbiome, bone mass, and CVD risk factors in adult women.

What is the current status of trial NCT04431960?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 51 participants. The study started on 2021-07-20. Estimated completion is 2022-10-03.

What interventions are being tested in trial NCT04431960?

The interventions under investigation include: blackcurrant (BC) extract (DRUG).

Who is sponsoring clinical trial NCT04431960?

This trial is sponsored by University of Connecticut, which has 107 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04431960's enrollment target sits among peer trials

51 969th of 2000 higher than 1,028 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02701153 · 51 participants · NA

    Phase II Study of 5-Day Hypofractionated Preoperative Radiation Therapy for Soft Tissue Sarcomas: Expansion Cohort

  • NCT03663790 · 51 participants · NA

    Effects of Gait Retraining on Lower Extremity Biomechanics

  • NCT03874052 · 51 participants · Phase 1

    Ruxolitinib in Combination With Venetoclax With and Without Azacitidine in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia

  • NCT04704661 · 51 participants · Phase 1

    Testing the Combination of Two Anti-cancer Drugs, DS-8201a and AZD6738, for The Treatment of Advanced Solid Tumors Expressing the HER2 Protein or Gene, The DASH Trial

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04431960, the US trial registry maintained by the National Library of Medicine. NCT04431960 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.