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Study on the clinical effect of moxibustion combined with eight-shells ointment on the prevention and treatment of complications in post-partum women--A Randomized Clinical Trial

Study on the clinical effect of moxibustion combined with eight-shells ointment on the prevention and treatment of complications in post-partum women--A Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000886
Enrollment
Unknown
Registered
2025-05-01
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Complications for women in the postnatal period

Interventions

test group:Conventional Treatment + Moxibustion Combined with Barsa Cream Treatment

Sponsors

Dongguan Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
21 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) Mothers who give birth vaginally; (2) Full-term, single foetus, head first; (3) Aged between 21 and 40 years old; (4) Breastfeeding with mother and baby in the same room after delivery; (5) The patient has not used any other medication or therapeutic measures related to the treatment of this disease during the treatment period;

Exclusion criteria

Exclusion criteria: Exclusion criteria: (1) Combined haemorrhage due to post-partum infection; (2) Postpartum intrauterine tissue retention; (3) Suffering from mental illness or family history of tumour, or medical or surgical diseases, neurological diseases, breast dysplasia, genitourinary related diseases, infectious diseases, and long-term medication; (4) Allergy to multiple drugs, moxibustion or being an allergic person, skin diseases, infectious diseases. (5) Those who did not meet the inclusion criteria, did not receive medication and adjuvant therapy as prescribed, could not judge the clinical efficacy or had incomplete information, etc., which affected the judgement of efficacy and safety, and those who had metallic substances (e.g., cardiac pacemakers) in their bodies; (6) Psychiatric or psychological disorders, traumatic events or communication disorders within the past 3 years.

Design outcomes

Primary

MeasureTime frame
postnatal abdominal pain;

Secondary

MeasureTime frame
postnatal constipation;postnatal incontinence;incessant postnatal discharge;lack of breast milk after childbirth;postpartum depression;postnatal urinary retention;Recovery from perineal lacerations;postnatal fatigue;;

Countries

China

Contacts

Public ContactYULIAN LIANG

Dongguan Hospital of Traditional Chinese Medicine

3284458150@qq.com13532755537

Outcome results

None listed

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