Efficacy of Ginger Extract (Compare Between the Ginger Preparation of Ancient Concept of Thai Traditional Practitioner, Standard Drug and Placebo) by Using Pain Score to Evaluate After Pain of Three Groups of First Normal Postpartum Women.
Primary Purpose
Postpartum Disorder
Status
Completed
Phase
Phase 1
Locations
Thailand
Study Type
Interventional
Intervention
Ginger
Placebo oral capsule
Paracetamol
Sponsored by
About this trial
This is an interventional treatment trial for Postpartum Disorder focused on measuring ginger extract, pain relief, postpartum women
Eligibility Criteria
Inclusion Criteria:
- Female.
- Being 20-34 years of age.
- First normal, healthy showing no symptoms of disorder. No history of toxemia of pregnancy, liver disease, kidney disease and gastrointestinal bleeding during pregnancy or after participating in a research project.
- Healthy pregnant women.
- No postpartum hemorrhage.
- Agrees to consent form.
- No need to take medication regularly.
- No smoking, no drinking alcohol during pregnancy.
Exclusion Criteria:
- Unable to travel conveniently.
- Allergic to modern medicine or herbal remedies.
- Have a gallstone problem.
Sites / Locations
- Naphatsaran Roekruangrit
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Placebo Comparator
Experimental
Active Comparator
Arm Label
Placebo
Ginger
Paracetamol
Arm Description
Outcomes
Primary Outcome Measures
Change in Pain Scores on the numeric rating scale at 3 days
measurement tool is numeric rating scale: NRS. Score from 0 to 10. Inclusion criteria start at Pain was classified as Mild (1-3), Moderate (4-6), and Severe (7-10).
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03617900
Brief Title
Efficacy of Ginger Extract (Compare Between the Ginger Preparation of Ancient Concept of Thai Traditional Practitioner, Standard Drug and Placebo) by Using Pain Score to Evaluate After Pain of Three Groups of First Normal Postpartum Women.
Official Title
EFFICACY OF GINGER EXTRACT ON PAIN RELIEF FOR FIRST NORMAL POSTPARTUM WOMEN
Study Type
Interventional
2. Study Status
Record Verification Date
May 2019
Overall Recruitment Status
Completed
Study Start Date
August 29, 2018 (Actual)
Primary Completion Date
May 25, 2019 (Actual)
Study Completion Date
May 25, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Thammasat University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Introduction A common problem in women after childbirth is bleeding (5-8 percent). This is one of the leading causes of maternal death in Thailand. The incidence of postpartum hemorrhage is approximately 1-2 percent of the births. A second problem is infection after birth which is a leading cause of illness and death of the mother. Incidence of infection after childbirth is 1-2 percent of women in developed countries and 5-10 percent of postpartum women overall. Staphylococcus aureus bacterium is found in the reproductive system of 5-9 percent of women. Perineal wound infections cause perineal pain. Thirdly is the problem of insufficient milk in foreign countries, mothers breastfeeding for less than 12 months total 94.7 percent. The fourth problem is difficult urination after vaginal delivery or 6 hours after removing the catheter in surgical cases. It is a common and important problem from 1.7 to 17.9 percent. The above problem causes infection and inflammation pain.
The first 24 hours after birth to 6 weeks physical and physiological changes of maternal organs and systems occurs such as the decline in hormone levels. This includes human placental lactogen (HPL), human chorionic somatomammotropin (HCS), human chorionic gonadotropin (HCG), estrogen, progesterone, prolactin, follicular stimulating hormones, luteinizing hormones. There is also blood loss. The clinical difficulties found in the postpartum period include after pain, perineal pain, breast engorgement, puerperal diuresis, weight loss, fever, pain and discomfort after birth. And the pain decreases or is lost in 3 days after birth.
The original gate-control theory proposed that there is a physiological within the substantia gelatinosa of the spinal cord's dorsal horn grey matter. It is suggested that sensory signals can only pass through the cells in the substantia gelatinosa when the gate is open. When the gate is closed, sensory information is blocked, and this forms the basis of a kind of physiological pain relief.
In relation to the 4 basic life elements of earth, water, wind and fire, the maternal body is lacking wind. This causes the fire to also decrease and the element of pain results. It becomes important to restore balance by stimulating blood circulation and herbal treatment is desirable to help the fire of the blood to speed the element of wind through the body.
Thai Traditional Medicine is used to treat the pain of mothers after childbirth. Because of in balance of mind fire in the body. By this reason, the balance of fire and wind increase to spread the circulatory system. Medicinal plants can increase the element of fire and the wind. Also, in Thai Traditional Medicine concept, pain reduction for postpartum mothers includes regular massage, herbal steam, herbal breast compress, Tub Mhor Kluer, eating heat-producing food. In the Thai Traditional Medicine manuscript, Kam-pee Mahachotharat there are 85 remedies for blood treatment therapy and especially, 44 contain ginger. Representing 51.76 percent of then.
Ginger has been included in the National Essential Medicines Catalogue 2554. Medication to relieve heartburn, bloating and distension, is documented and prevention and relief of nausea and vomiting due to motion sickness, seasickness. Or after surgery, are all included.
Detailed Description
1.2 Objectives
1.2.1 Primary Objective To compare the efficacy of ginger extract on pain relief at the following anatomical locations. Uterus, episiotomy and breast.
1.2.2 Secondary Objectives 1.2.2.1 To study the biological activity and stability of ginger extract. 1.2.2.2 To compare pain scores by using ginger extract for first normal postpartum women.
1.3 Benefit of Output 1.3.1 Knowledge on standard and the stability of ginger extract. 1.3.2 Knowledge on the effectiveness of ginger extract on pain relief for first normal postpartum women.
1.3.3 Knowledge on clinical research of pain relief for first normal postpartum women in the next big group volunteers.
1.3.4 Agencies involved in the field of conventional medicine and Thai Traditional Medicine may use results for study, further research and development of new drugs.
1.4 Operational Definition 1.4.1 Efficacy of ginger extract referred to changes result from receive ginger extract.
1.4.2 Pain referred to IASP (International Association for the Study of Pain) pain that persists beyond normal healing time p>24 hours.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Postpartum Disorder
Keywords
ginger extract, pain relief, postpartum women
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
99 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Title
Ginger
Arm Type
Experimental
Arm Title
Paracetamol
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Ginger
Intervention Description
Ginger extract is contains 100 mg/capsules. Use 2 capsules 3 times/day
Intervention Type
Drug
Intervention Name(s)
Placebo oral capsule
Intervention Description
Lactose monohydrate 400 mg/capsules
Intervention Type
Drug
Intervention Name(s)
Paracetamol
Intervention Description
500 mg paracetamol. use in need
Primary Outcome Measure Information:
Title
Change in Pain Scores on the numeric rating scale at 3 days
Description
measurement tool is numeric rating scale: NRS. Score from 0 to 10. Inclusion criteria start at Pain was classified as Mild (1-3), Moderate (4-6), and Severe (7-10).
Time Frame
2 hours after delivery time and be continued every 6 hours for 3 days.
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
34 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Female.
Being 20-34 years of age.
First normal, healthy showing no symptoms of disorder. No history of toxemia of pregnancy, liver disease, kidney disease and gastrointestinal bleeding during pregnancy or after participating in a research project.
Healthy pregnant women.
No postpartum hemorrhage.
Agrees to consent form.
No need to take medication regularly.
No smoking, no drinking alcohol during pregnancy.
Exclusion Criteria:
Unable to travel conveniently.
Allergic to modern medicine or herbal remedies.
Have a gallstone problem.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Preecha Wanichsetakul, M.D.
Organizational Affiliation
Thammasat University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Arunporn Itharat, PH.D.
Organizational Affiliation
Thammasat University
Official's Role
Study Chair
Facility Information:
Facility Name
Naphatsaran Roekruangrit
City
Pathumthani
ZIP/Postal Code
12121
Country
Thailand
12. IPD Sharing Statement
Citations:
PubMed Identifier
33078388
Citation
Deussen AR, Ashwood P, Martis R, Stewart F, Grzeskowiak LE. Relief of pain due to uterine cramping/involution after birth. Cochrane Database Syst Rev. 2020 Oct 20;10(10):CD004908. doi: 10.1002/14651858.CD004908.pub3.
Results Reference
derived
Learn more about this trial
Efficacy of Ginger Extract (Compare Between the Ginger Preparation of Ancient Concept of Thai Traditional Practitioner, Standard Drug and Placebo) by Using Pain Score to Evaluate After Pain of Three Groups of First Normal Postpartum Women.
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