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Clinical Trials/JPRN-jRCT1051190012
JPRN-jRCT1051190012CompletedPhase 4

A prospective interventional study of Japanese herbal medicine, Ninjin-Youei-To on preoperative anemia and fatigue, insomnia and anxiety in patients who receive gynecologic operation - Ninjin-Youei-To study

Kimura Tadashi0 sites40 target enrollmentStarted: April 28, 2019Last updated:
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Conditions

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
40
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The combined use of NYT and iron supplementation for anemia before surgery for gynecological diseases improved patients' anemia as much as iron supplementation alone. Moreover, the combination therapy significantly alleviated their fatigue and anxiety. Thus, this combination therapy can be an effective treatment option in gynecological care.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
>= 20age old to ot applicable (—)
Sex
Female

Inclusion Criteria

  • •Patients who receive gynecologic operation and take Ferromia by diagnosing as anemia (Hb less than 11g/dl)
  • •They subject with age more than 20 years

Exclusion Criteria

  • •1. Patients with concomitant use of other Japanese herbal medicine
  • •2. Patients with use of Japanese herbal medicine for fatigue, insomnia and anxiety within two weeks
  • •3. Patients with depression
  • •4. Patients with aldosteronism, myopathy and hypokalemia
  • •5. Patients with liver dysfunction(AST more than 80 IU/L or ALT more than 80 IU/L)
  • •6. Patients who are inappropriate to participate in the study

Investigators

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