Evidence map›Paper›PMID 42774549›Full record

ArticleInternational journal of reproductive biomedicine2026

Oral dydrogesterone versus oral micronized progesterone: Interim analysis of a randomized controlled trial in pregnant women with threatened miscarriage.

Alka Kriplani, Ashima Taneja, Gouri Shankar Kamilya, Thirunavukkarasu Ramani Devi, Amol Pawar, Tanusree Gupta, Gayathri Karthik Nagesh, Shilpa Choudhary, Tapan Pattanaik, Monjori Mitra

Abstract read
In one paragraph

Article in International journal of reproductive biomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Alka KriplaniDepartment of Obstetrics and Gynecology, Paras Hospitals, Gurugram, Haryana, India.
Ashima TanejaDepartment of Obstetrics and Gynecology, Dayanand Medical College & Hospital, Ludhiana, Punjab, India.
Gouri Shankar KamilyaDepartment of Obstetrics and Gynecology, IPGME&R and SSKM Hospital, Kolkata, West Bengal, India.
Thirunavukkarasu Ramani DeviDepartment of Obstetrics and Gynecology, Ramakrishna Medical Center LLP, Tiruchirappalli, Tamil Nadu, India.
Amol PawarDepartment of Obstetrics and Gynecology, Nowrosjee Wadia Maternity Hospital, Mumbai, Maharashtra, India.
Tanusree GuptaDepartment of Gynecology and Obstetrics, Udyan Health Care Pvt. Ltd., Lucknow, Uttar Pradesh, India.
Gayathri Karthik NageshDepartment of Obstetrics and Gynecology, Manipal Hospital, Bengaluru, Karnataka, India.
Shilpa ChoudharyLifeline Medicare Hospital, Mumbai, Maharashtra, India.
Tapan PattanaikDepartment of Obstetrics and Gynecology, Sum Ultimate Medicare Hospital, Bhubaneswar, Odisha, India.
Monjori MitraDepartment of Pediatrics, Institute of Child Health, Kolkata, West Bengal, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Progestogen/progestin supplementation is favorable in threatened miscarriage. However, comparative data on the efficacy, safety, and immunomodulatory functions of types/routes of administration are limited. Objective: This study compares oral dydrogesterone (DYD) vs. oral micronized progesterone (MP) in threatened miscarriage. Materials and Methods: This ongoing, investigator-initiated, randomized controlled trial includes eligible, consenting, pregnant women who had vaginal bleeding and/or abdominal pain during first trimester. Participants are treated up to 14 gestational wk with DYD (40 mg stat followed by 10 mg thrice daily) or MP (200 mg twice daily). The following outcomes till 20 gestational wk are presented: miscarriage rate (primary); change in serum cytokines (interferon gamma [IFN- Results: Interim analysis includes 116 participants (DYD, 62; MP, 54). Miscarriage rate in DYD (14.52%) was statistically comparable to, but numerically lower than, that in MP (20.37%; p = 0.558). The mean time to symptom resolution in DYD and MP was, respectively, 6.49 and 7.38 days for vaginal bleeding, and 7.15 and 7.67 days for abdominal pain. Numerically, IFN- Conclusion: Compared to oral MP, oral DYD resulted in a numerically lower miscarriage rate and time to symptom resolution, concomitant to favorable decrease in Th1:Th2 ratio.

Indexed as

DydrogesteronePregnancy complicationsProgesteroneRandomized controlled trial.Threatened miscarriage

Identifiers

PMID42774549
PMCPMC13594364

What Socratic holds

Textmetadata
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.