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COMPLETED NA

Transcutaneous Electrical Nerve Stimulation (TENS) for Pain Control During First Trimester Abortion

NCT03187002 · View on ClinicalTrials.gov ↗

Study Summary

High-frequency, high-intensity transcutaneous electrical nerve-stimulation (TENS) is an inexpensive and non-invasive pain control approach. TENS, pulsating electrical currents that activate underlying nerves, does not have drug interactions or risk of overdose. Cochrane review of TENS for acute pain found inconclusive evidence. One previous abortion trial comparing TENS to IV sedation only looked at pain control in the recovery room. The investigators propose a randomized controlled trial comparing TENS to IV sedation (in conjunction with local anesthesia) among women presenting for first-trimester surgical abortion. Primary outcome will be perceived pain by Visual Analogue Scale (VAS) during aspiration.

Interventions

  • DEVICE Transcutaneous electrical nerve stimulation (TENS)
  • DRUG Moderate IV Sedation
  • OTHER SHAM: Transcutaneous electrical nerve stimulation (TENS)
  • OTHER SHAM: Moderate IV Sedation

Study Locations (1)

California

  • Planned Parenthood Mar Monte — San Jose

Trial Details

FieldValue
Enrollment Target 109 participants
Start Date 2018-01-18
Est. Completion 2019-10-31
Phase NA

Sponsor

Stanford University

1,643 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03187002

The ClinicalTrials.gov registry entry for NCT03187002 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 109 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Stanford University, which has 1,643 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Abortion in First Trimester appearing as the primary indexed condition, and to 4 interventions — of which Transcutaneous electrical nerve stimulation (TENS) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03187002 reports 1 study location spanning 1 distinct geographic area — top geographies include California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03187002 about?

NCT03187002 is a clinical study titled "Transcutaneous Electrical Nerve Stimulation (TENS) for Pain Control During First Trimester Abortion". High-frequency, high-intensity transcutaneous electrical nerve-stimulation (TENS) is an inexpensive and non-invasive pain control approach. TENS, pulsating electrical currents that activate underlying nerves, does not have drug interactions or risk of overdose. Cochrane review of TENS for acute pain...

What is the current status of trial NCT03187002?

This trial is currently completed. It is a NA study. The enrollment target is 109 participants. The study started on 2018-01-18. Estimated completion is 2019-10-31.

What conditions does trial NCT03187002 study?

This clinical trial studies the following conditions: Abortion in First Trimester. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03187002?

The interventions under investigation include: Transcutaneous electrical nerve stimulation (TENS) (DEVICE), Moderate IV Sedation (DRUG), SHAM: Transcutaneous electrical nerve stimulation (TENS) (OTHER), SHAM: Moderate IV Sedation (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03187002?

This trial is sponsored by Stanford University, which has 1,643 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03187002 being conducted?

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

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial