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Clinical observation of percutaneous acupoint electrical stimulation for uterine contraction pain after Yin delivery

Clinical observation of percutaneous acupoint electrical stimulation for uterine contraction pain after Yin delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079910
Enrollment
Unknown
Registered
2024-01-16
Start date
2024-01-30
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Buterine pain after Yin delivery

Interventions

Trial group:Electrical stimulation was carried out on the left ridge and left side, right ridge and right side, left ground and left three yin. Adjustment parameters: thin wave 2 Hz, dense wave 30 Hz,
Control group:No electrical stimulation of the transcutaneous acupoints

Sponsors

Jinan Maternal and Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
22 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1) The maternal age is 22 to 35 years, gestational age is 37-42 weeks; 2) Blood routine, heart, liver, and kidney function, no serious abnormalities; 3) No mental illness, no intellectual obstruction, fluent language, normal communication, the ability to judge their own pain and general condition; 4) The maternal or her relatives signed informed consent.

Exclusion criteria

Exclusion criteria: 1) With intentional, liver, lung, kidney, hematopoietic system, and other diseases; 2),With mental disorders, limb hemiplegia, or lower limb sensory disorders; 3),With serious complications during pregnancy; 4) Using other drugs or non-drug analgesia.

Design outcomes

Primary

MeasureTime frame
Numeric Rating Scale;

Secondary

MeasureTime frame
The degree of uterine recovery;Postpartum contractions and pain time;

Countries

China

Contacts

Public ContactYaqiu Guo

Jinan Maternal and Child Health Care Hospital

guoyaqiu0055@163.com+86 180 5315 8617

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026