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Effect of Postpartum Manual Lymphatic Drainage Combined with Pelvic Floor Myofascial Release on the Resolution of Perineal Edema Following Vaginal Delivery: A Randomized Controlled Trial

Effect of Postpartum Manual Lymphatic Drainage Combined with Pelvic Floor Myofascial Release on the Resolution of Perineal Edema Following Vaginal Delivery: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104489
Enrollment
Unknown
Registered
2025-06-18
Start date
2025-06-30
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Edema of the perineal or vulvar region caused by pregnancy and childbirth

Interventions

Experimental Group:Manual Lymphatic Drainage Combined with Pelvic Floor Myofascial Release Therapy
Control Group:Standard Clinical Nursing Care

Sponsors

Southern Medical University Southern Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Women undergoing vaginal delivery; 2.Women with full-term singleton pregnancies; 3.Women with cephalic fetal presentation; 4.Women aged over 18 years; 5.Women diagnosed with first- or second-degree perineal lacerations, or who underwent episiotomy; 6.Women presenting with perineal and/or vulvar edema; 7.Women without urogenital complications; 8.Women who voluntarily signed the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Women with major comorbidities (e.g., heart disease, systemic lupus erythematosus); 2.Women with perineal hematoma, wound infection, or varicose veins; 3.Women with retained placenta or membranes; 4.Women who used analgesics or non-steroidal anti-inflammatory drugs (NSAIDs) postpartum; 5.Women who were separated from their newborns postpartum; 6.Patients deemed unsuitable for participation by the investigators; 7.Women with hypoproteinemia (total serum protein < 60 g/L or albumin < 35 g/L).

Design outcomes

Secondary

MeasureTime frame
Perineal Healing Status;Pain;Level of postnatal self-care;

Primary

MeasureTime frame
Perineal/Vulvar Edema Size;

Countries

China

Contacts

Public ContactXue Xu

Southern Medical University Southern Hospital

383683764@qq.com+86 13430344939

Outcome results

None listed

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