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Effectiveness of Ayurved Siriraj Prasa-Nam-Nom Recipe on Breast Milk Volume in Early Postpartum Women: a randomized, double-blind, placebo-controlled trial

Effectiveness of Ayurved Siriraj Prasa-Nam-Nom Recipe on Breast Milk Volume in Early Postpartum Women: a randomized, double-blind, placebo-controlled trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190218004
Enrollment
Unknown
Registered
2019-02-18
Start date
2012-08-26
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

early postpartum women creamatocrit galactagogue prolactin inadequate breast milk volume

Interventions

ASPNN recipe 500 mg per capsule,fine granular flour&#44
magnesium stearate and talcum 500 mg in the identical capsule shells
Experimental Dietary Supplement,Placebo Comparator No treatment
ASPNN,Placebo

Sponsors

Siriraj Research Development Fund (Managed by Routine to Research : R2R)
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) age of >18 years old (2) first vaginal delivery at term (3) inadequate milk volume (0-49 ml/breast pump)

Exclusion criteria

Exclusion criteria: (1) having medical disorders, such as hypertension, type 2 diabetes, thyrotoxicosis and hypothyroidism (2) previous allergy to ASPNN or its ingredients (3) inability to eat vegetables or spicy food (4) severe breastfeeding problems, such as abnormal breast anatomy, short nipples, mastitis, breast abscess and severe fetal tongue-tie (5) taking galactagogue, such as domperidone, metoclopramide, antidepressive drugs, caffeine and alcohol

Design outcomes

Primary

MeasureTime frame
breast milk production on day 1 and day 3 after the intervention Volume by an electrical breastpump and a measuring flask

Secondary

MeasureTime frame
milk quality on day 1 and day 3 after the intervention cream percentage (creamatocrit) ,serum prolactin level on day 1 and day 3 after the intervention Prolactin II assay,safety of the intervention on day 3 observed unwanted effects

Countries

Thailand

Contacts

Public ContactThapthep Thippayacharoentam

Center of Applied Thai Traditional Medicine, Faculty of Medicine Siriraj Hospital, Mahidol Universit

reab.tip@mahidol.edu+66+02+4198906

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026