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ANSiStim Study for Active Labor Pain

Study of ANSiStim for Pain Relief During Active Labor Phase Through Continues Checking of VAS SCORE

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02427139
Acronym
ANSS-ALP
Enrollment
50
Registered
2015-04-27
Start date
2015-03-31
Completion date
2016-09-30
Last updated
2016-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Labor Pain, Obstetric Pain

Brief summary

The specific aim of the study is to do comparison between ANSiStim and Placebo for pain relief in labor. During the treatment, pain relief will be assesed with ANSiStim in active labor through continues checking of VAS SCORE. ANSiStim has been tried in post operative patients with good pain relief .

Detailed description

Pain during labor is caused by contractions of the muscles of the uterus and by pressure on the cervix. This pain can be felt as strong cramping in the abdomen, groin, and back, as well as an achy feeling. Some women experience pain in their sides or thighs as well. Most women have an epidural or spinal during labour or after the birth.

Interventions

DEVICEANSiStim

ANSiStim allows continuous point stimulation over a period of several days while offering the patient a high degree of comfort and mobility at the same time. Use of the ANSiSTIM therapy provides overwhelming advantage over drug therapy minimizing possible side-effects caused by pain medications (i.e. opioid) such as, for example, impaired reactions. In most cases, the patient continues to lead its life as normal, without side effects or any loss of quality of life.

Sponsors

DyAnsys, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Pregnant Women on an Active Labor

Exclusion criteria

* Cardiac Pacemaker or any other implants * Psoriasis * Diminish mental capacity

Design outcomes

Primary

MeasureTime frame
Evidence of Reduced Pain (Pain Scale of 5) in Active Labor Phase after ANSiStim Placement48 Hours

Countries

India

Contacts

Primary ContactMurugesh K
k.murugesh@dyansys.com04428133748
Backup ContactJithesh RP, M.B.A.
r.p.jithesh@dyansys.com7708931316

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026