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

NCT04557553 · ClinicalTrials.gov registry record · NA

Effects of Lagenbone on Bone Mineral Density

A NA study of Osteoporosis, sponsored by Southern California University of Health Sciences.

Completed
Registry status
NA
Development phase
10
Enrollment target
1
Study location

NCT04557553: Completed NA study of Osteoporosis, sponsored by Southern California University of Health Sciences.

NCT04557553 is a NA study of Osteoporosis that has completed, run by Southern California University of Health Sciences. The registered enrollment target is 10 participants, below the 1,546-participant average among 84 other Osteoporosis trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04557553, a NA study of Osteoporosis, has completed, sponsored by Southern California University of Health Sciences.

COMPLETED
Registry status
NA
Development phase
10 participants
Enrollment target
1
Study location

Study Summary

To study the effects of the herbal supplement Lagenbone on Bone Mineral Density

Primary Outcome

Dual-energy x-ray absorptiometry (DXA) or bone densitometry or Bone Density Scan

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT Lagenbone

Study Locations (1)

California

  • Southern California University of Health Sciences - Whittier

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2019-07-15
Est. Completion 2022-07-13
Phase NA

What the finished NCT04557553 record still lists

NCT04557553 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 1,546-participant average among 84 other Osteoporosis trials with a reported enrollment target (99% lower).

The record links to 1 condition, with Osteoporosis appearing as the primary indexed condition, and to 1 intervention - of which Lagenbone is the first listed.

NCT04557553 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT04557553 about?

NCT04557553 is a clinical study titled "Effects of Lagenbone on Bone Mineral Density". To study the effects of the herbal supplement Lagenbone on Bone Mineral Density

What is the current status of trial NCT04557553?

This trial is currently completed. It is a NA study. The enrollment target is 10 participants. The study started on 2019-07-15. Estimated completion is 2022-07-13.

What conditions does trial NCT04557553 study?

This clinical trial studies the following conditions: Osteoporosis.

What interventions are being tested in trial NCT04557553?

The interventions under investigation include: Lagenbone (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT04557553?

This trial is sponsored by Southern California University of Health Sciences, which has 10 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04557553 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Osteoporosis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT04557553's enrollment target sits among peer trials

10 83rd of 84 higher than 1 of 84 other Osteoporosis trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Osteoporosis 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

  • NCT00623389 · 10 participants · NA

    Evaluation of an Advanced Lower Extremity Neuroprostheses

  • NCT01241864 · 10 participants · Phase 2

    Islet Transplantation in Type 1 Diabetic Kidney Allograft

  • NCT01293214 · 10 participants · NA

    Vascularized Composite Allotransplantation for Multiple Extremity Amputations

  • NCT01474148 · 10 participants · NA

    A Neuroprosthesis for Seated Posture and Balance

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 NCT04557553, the US trial registry maintained by the National Library of Medicine. NCT04557553 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.