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NCT01960946 · ClinicalTrials.gov registry record · NA

Galectin-3 Blockade in Patients With High Blood Pressure

A NA study, sponsored by Massachusetts General Hospital.

Completed
Registry status
NA
Development phase
59
Enrollment target

NCT01960946: Completed NA study, sponsored by Massachusetts General Hospital.

NCT01960946 is a NA study that has completed, run by Massachusetts General Hospital. The registered enrollment target is 59 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT01960946, a NA study, has completed, sponsored by Massachusetts General Hospital.

COMPLETED
Registry status
NA
Development phase
59 participants
Enrollment target

Study Summary

This study will investigate if Modified Citrus Pectin (MCP) can help people with high blood pressure. MCP is a dietary supplement that is derived from plants, and therefore is not subject to approval by the U.S. Food and Drug Administration (FDA). However, MCP has been deemed as 'generally regarded as safe' by the FDA. This study will examine whether Modified Citrus Pectin (MCP) can help people with high blood pressure. The study will help understand how MCP may affect the risk for heart disease in patients with high blood pressure.

Primary Outcome

Primary aim will be change in markers of collagen metabolism (PICP, PIIICP, ICTP, TIMP-1) in MCP versus placebo groups over 6 months of treatment.

Interventions

  • DIETARY_SUPPLEMENT Modified Citrus Pectin (MCP) vs placebo

Trial Details

FieldValue
Enrollment Target 59 participants
Start Date 2013-10
Est. Completion 2018-08-30
Phase NA
Massachusetts General Hospital

2,032 total trials

What the finished NCT01960946 record still lists

NCT01960946 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 59 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 1 intervention - of which Modified Citrus Pectin (MCP) vs placebo is the first listed.

NCT01960946 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01960946 about?

NCT01960946 is a clinical study titled "Galectin-3 Blockade in Patients With High Blood Pressure". This study will investigate if Modified Citrus Pectin (MCP) can help people with high blood pressure. MCP is a dietary supplement that is derived from plants, and therefore is not subject to approval by the U.S. Food and Drug Administration (FDA). However, MCP has been deemed as 'generally regarded ...

What is the current status of trial NCT01960946?

This trial is currently completed. It is a NA study. The enrollment target is 59 participants. The study started on 2013-10. Estimated completion is 2018-08-30.

What interventions are being tested in trial NCT01960946?

The interventions under investigation include: Modified Citrus Pectin (MCP) vs placebo (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT01960946?

This trial is sponsored by Massachusetts General Hospital, which has 2,032 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01960946's enrollment target sits among peer trials

59 1256th of 2000 higher than 745 of 2,000 other NA trials

participants (enrollment target), bucketed by value

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

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Source: ClinicalTrials.gov NCT01960946, the US trial registry maintained by the National Library of Medicine. NCT01960946 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.