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NCT06388590 · ClinicalTrials.gov registry record · NA

Acupuncture for Chronic Pelvic Pain

A NA study of Pelvic Pain and Acupuncture, sponsored by David Moss.

Recruiting
Registry status
NA
Development phase
64
Enrollment target
1
Study location

NCT06388590: Recruiting NA study of Pelvic Pain and Acupuncture, sponsored by David Moss.

NCT06388590 is a NA study of Pelvic Pain and Acupuncture that is actively recruiting participants, run by David Moss. The registered enrollment target is 64 participants, below the 369-participant average among 23 other Pelvic Pain trials with a reported enrollment target (83% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06388590, a NA study of Pelvic Pain and Acupuncture, is actively recruiting participants, sponsored by David Moss.

RECRUITING
Registry status
NA
Development phase
64 participants
Enrollment target
1
Study location

Study Summary

The objective of this study is to determine if alternative pain management strategies, namely acupuncture, may help reduce intensity of female pelvic pain compared to other pain control modalities. This research study will focus specifically on the Dragon's protocol of acupuncture which will seek to alleviate chronic non-endometriosis pelvic pain for women both with and without a history of sexual assault. This study may support evidence for an inexpensive alternative means of treatment for patients with or without traumatic sexual history and chronic pelvic pain.

Primary Outcome

The DVPRS consists of an 11-point numerical rating scale with 0 indicating no pain and 10 indicating severe pain. It has been confirmed for reliability and validity in measuring both acute and chronic pain and is currently the standard for pain measurement throughout DoD and VA health systems. The DVPRS has demonstrated linear scale qualities allowing parametric methods to be used.

Interventions

  • OTHER Standard of Care
  • OTHER Dragons

Study Locations (1)

Nevada

  • Mike O'Callaghan Military Medical Center - Nellis Air Force Base

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2024-12-01
Est. Completion 2026-04
Phase NA
David Moss

7 total trials

What NCT06388590 shows while recruiting

NCT06388590 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 64 participants, a relatively small participant target, below the 369-participant average among 23 other Pelvic Pain trials with a reported enrollment target (83% lower).

The record links to 3 conditions, with Pelvic Pain appearing as the primary indexed condition, and to 2 interventions - of which Standard of Care is the first listed.

NCT06388590 reports a single indexed study location in Nevada.

Frequently Asked Questions

What is clinical trial NCT06388590 about?

NCT06388590 is a clinical study titled "Acupuncture for Chronic Pelvic Pain". The objective of this study is to determine if alternative pain management strategies, namely acupuncture, may help reduce intensity of female pelvic pain compared to other pain control modalities. This research study will focus specifically on the Dragon's protocol of acupuncture which will seek to...

What is the current status of trial NCT06388590?

This trial is currently recruiting. It is a NA study. The enrollment target is 64 participants. The study started on 2024-12-01. Estimated completion is 2026-04.

What conditions does trial NCT06388590 study?

This clinical trial studies the following conditions: Pelvic Pain, Acupuncture, Gynecology.

What interventions are being tested in trial NCT06388590?

The interventions under investigation include: Standard of Care (OTHER), Dragons (OTHER).

Who is sponsoring clinical trial NCT06388590?

This trial is sponsored by David Moss, which has 7 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06388590 being conducted?

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

Similar trials for Pelvic Pain

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 NCT06388590's enrollment target sits among peer trials

64 13th of 23 higher than 11 of 23 other Pelvic Pain trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Pelvic Pain 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 NCT06388590, the US trial registry maintained by the National Library of Medicine. NCT06388590 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.