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NCT03653988 · ClinicalTrials.gov registry record · NA

Comparison of Pre-op and Post-op Pectoralis Nerve Block

A NA study, sponsored by Melinda Seering.

Completed
Registry status
NA
Development phase
34
Enrollment target

NCT03653988: Completed NA study, sponsored by Melinda Seering.

NCT03653988 is a NA study that has completed, run by Melinda Seering. The registered enrollment target is 34 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03653988, a NA study, has completed, sponsored by Melinda Seering.

COMPLETED
Registry status
NA
Development phase
34 participants
Enrollment target

Study Summary

The investigators will compare whether patients will have better pain control if they were to receive (PEC I/II block) before surgery or after mastectomy.

Primary Outcome

The primary outcome to be assessed is to determine if there is a quantitative difference in post-operative pain scores as a result of the administration of a pre-operative PECS I/II block versus the administration of an intra-operative PECS I/II block (Post mastectomy but prior to breast reconstruction). The visual analog scale is a unidimensional measure of pain used in a diverse adult population. The numeric values are on a continuous scale from 0 to 10 with 0 indicating no pain, 5 being moder

Interventions

  • PROCEDURE PEC I/II blocks by anesthesiologist - pre-operative
  • PROCEDURE PEC I/II blocks by surgeon - intra-operative

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2019-03-12
Est. Completion 2021-10-31
Phase NA
Melinda Seering

3 total trials

What the finished NCT03653988 record still lists

NCT03653988 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 34 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which PEC I/II blocks by anesthesiologist - pre-operative is the first listed.

NCT03653988 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03653988 about?

NCT03653988 is a clinical study titled "Comparison of Pre-op and Post-op Pectoralis Nerve Block". The investigators will compare whether patients will have better pain control if they were to receive (PEC I/II block) before surgery or after mastectomy.

What is the current status of trial NCT03653988?

This trial is currently completed. It is a NA study. The enrollment target is 34 participants. The study started on 2019-03-12. Estimated completion is 2021-10-31.

What interventions are being tested in trial NCT03653988?

The interventions under investigation include: PEC I/II blocks by anesthesiologist - pre-operative (PROCEDURE), PEC I/II blocks by surgeon - intra-operative (PROCEDURE).

Who is sponsoring clinical trial NCT03653988?

This trial is sponsored by Melinda Seering, which has 3 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03653988's enrollment target sits among peer trials

34 1570th of 2000 higher than 427 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 NCT03653988, the US trial registry maintained by the National Library of Medicine. NCT03653988 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.