search
Back to results

Therapeutic Effect of Herbal Infusion on Menometrorrhagia (HERBALTREAT)

Primary Purpose

Abnormal Uterine Bleeding, Menorrhagia; Postmenopausal, Metrorrhagia

Status
Completed
Phase
Not Applicable
Locations
Tunisia
Study Type
Interventional
Intervention
Tea infusion
Sponsored by
Faculty of Medicine, Sousse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Abnormal Uterine Bleeding focused on measuring plants, Traditional herbal Medicine, Tisane

Eligibility Criteria

30 Years - 55 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women failed first-line intervention to stop bleeding and planned for hysterectomy
  • Women between (30-50 years)
  • Able to understand and provide informed consent to participate in the study.
  • Not pregnant or lactating
  • Having menstrual period more than 7 days with uterine bleeding at irregular intervals.

Exclusion Criteria:

Participants with at least one of the following criteria will not be included in the trial:

  • Chronic disease with long-term treatment (i.e. asthma, cardiovascular disorders..)
  • woman taking any standard medications for abnormal uterine bleeding
  • Women who have a history of gastrointestinal bleeding or ulcer
  • Women who have abnormal kidney function
  • Participants with increasing menstrual bleeding during the treatment requires surgical emergency procedures.
  • Those refusing the instructions or participating in other clinical trials.
  • Participant take other herbal treatment
  • - Age less than 18 years
  • - Healthy Volunteers
  • women with ovarian tumours

Sites / Locations

  • faculty of medicine Sousse

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Tea infusion

Arm Description

The aerial parts of each plant were dried, then, they were powdered in a rotating knife grinder. The herbs were taken as tea infusion by the oral route. the powder of the mixture was added to 100 ml of boiling water and the tea infusion was taken three times a day for three consecutive days and it was repeated for three consecutive months

Outcomes

Primary Outcome Measures

Reduce the menstrual duration in days
the Pictorial Blood Loss Assessment Chart (PBLAC) the number of bleeding day during menstruation
Reduce the bleeding abundance
bleeding abundance will be measured by the Pictorial Blood Loss Assessment Chart (PBLAC) The total score is calculated by adding up the sum of all scores for the sanitary pads used in the menstrual cycle. : 1 for lightly stained, 5 for moderately soiled, and 20 for completely saturated pads. Clots were given a score of 1 for small and 5 for large clots. Abnormal PBLAC bleeding score greater than or equal to 100, which correlates with bleeding abundance, defined as greater than 80 mL of menstrual blood loss. Normal bleeding is defined as a score of 75 or less. A score of 0 indicates amenorrhea or the absence of menstruation.

Secondary Outcome Measures

Change From Baseline in Hematocrit (Hct) Concentrations at Treatment Day 90
Hematocrit was measured before treatment and after 90 days at the end of treatment
Change From Baseline in Hemoglobin Concentration at Treatment Day 90
Hemoglobin was measured before treatment and after 90 day A positive value indicates an increase in hemoglobin from baseline at treatment day 90
Change From Baseline in Fibrinogen Concentration at Treatment Day 90
Fibrinogen Concentration was measured before treatment and after 90 day
Change From Baseline in Prothrombin Time at Treatment Day 90
Prothrombin Time was measured before treatment and after 90 day
hange From Baseline in serum Creatinine Time at Treatment Day 90
to detect urinary toxicity. conducted at the start of the trial and after the last infusion consumption days 90

Full Information

First Posted
December 24, 2021
Last Updated
June 4, 2022
Sponsor
Faculty of Medicine, Sousse
Collaborators
Centre Hôpital Universitaire Farhat Hached
search

1. Study Identification

Unique Protocol Identification Number
NCT05406960
Brief Title
Therapeutic Effect of Herbal Infusion on Menometrorrhagia
Acronym
HERBALTREAT
Official Title
The Therapeutic Effect of Traditional Herbal Tea Infusion on Abnormal Uterine Bleeding- Menometrorrhagia
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
May 10, 2019 (Actual)
Primary Completion Date
December 20, 2020 (Actual)
Study Completion Date
February 10, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Faculty of Medicine, Sousse
Collaborators
Centre Hôpital Universitaire Farhat Hached

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is an interventional, non-randomized, controlled, pilot study that explores a new approach to treat, Abnormal uterine bleeding-menometrorrhagia in women, being candidates for hysterectomy, based on tea infusion consumption of a mixture of two plants.
Detailed Description
Menometrorrhagia is excessive uterine bleeding resulting from a combination of two different conditions, namely menorrhagia, which is heavy bleeding during the menstrual period, and metrorrhagia, when the period lasts more than seven days or when uterine bleeding exists between periods. It is defined as abnormal uterine bleeding (AUB) and it is a worldwide health problem affecting 11 to 13% of the general female population in the reproductive age and increasing up to 24% in women aged 40-50 years. Conventional treatment of menometrorrhagia consists of symptomatic treatment including tranexamic acid and levonorgestrel intrauterine device. If the first-line medication fails to treat women with AUB, surgical treatment such as a hysterectomy could be necessary. However, both medical treatments and surgical procedures have different side effects, including gastrointestinal symptoms, liver disease, obesity, and thromboembolic diseases. Moreover, the hypoestrogenic state of these therapies can also lead to rapid bone demineralization and menopausal symptoms, such as vaginal dryness and hot flushes, having a negative effect on women's quality of life. Thus, because of these serious side effects, it seems logical to investigate other available sources. Such problems may be beyond the scope of herbal treatment. Mentha pulegium is a perennial plant from the Lamiaceae family, also known as Pennyroyal, and is used in pharmaceutical and agro-alimentary industries. Artemisia abrotanum L, commonly known as Southernwood, is a small bushy shrub with small, feathery, narrow, and grey-green leaves. The genus belongs to the Asteraceae family. A mixture of these two herbs is known as a strong emmenagogue. Data collection: The plants used in this study were collected through an ethnobotanical survey. The data on the plants' studies were collected through an internet search in: Medicinal plants mentioned in Canon www., www. Science Direct, www.pubmed.com. , www. Scopus, www.wiley.com, www. Google scholar, www. web of science, books in phytotherapy All details with regard to : The effect of the treatment on the menstrual cycle Menstruation duration Adverse effects Bleeding intensity measured using Pictorial Blood Assessment Chart during three consecutive menstrual treatments and the three-month follow-up. will be collected from participants by phone Details about the Follow-up: Allocated to intervention : Follow-up (Visit 2): Phone or direct contact after the end of oral administration (day 3) for clinical response evaluation. Phone or direct contact one week after treatment Follow-up 3: Phone or direct contact after the end of oral administration (day 3) for clinical response evaluation. Phone or direct contact one week after treatment Follow-up (Visit 4): Phone or direct contact after the end of oral administration (day 3) for clinical response evaluation. Phone or direct contact one week after treatment VISIT 5 (closing visit) Statistical Analysis Data entry and analysis will be performed using ( IBMV SPSS R 20.0). To test for normality and distribution of the variables. A significance level of a p-value of less than 0.05 will be considered Descriptive statistics will be used to examine the characteristics of the study population (means, standard deviation). Comparison of the biological parameters and scores of PBAC between baseline and the end of treatment will be performed using paired t-test when variables are normally distributed and Wilcoxon signed ranks test, as a non-parametric test when variables are not normally distributed. Sample size The sample size will be assessed according to the following formula N = (Zα/2) 2 s2 /d2, where "s" is the standard deviation (SD ). "d" is the accuracy of the estimate. "Zα/2" is the normal deviate for a two-tailed alternative hypothesis at a level of significance.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Abnormal Uterine Bleeding, Menorrhagia; Postmenopausal, Metrorrhagia, Hysterectomy, Heavy Menstrual Bleeding
Keywords
plants, Traditional herbal Medicine, Tisane

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
The gynecologist who decided if the participant met the selection criteria or not Participants meeting the selection criteria will be included in the study. Before starting all the included participants underwent a complete physical examination. Written informed consent will be obtained. The herbal tea infusion will be self-administrated by participants at home. Participants will receive training on how to make herbal tea infusions at home. Participants will be interviewed by the investigator of the study: To complete a quality-of-life questionnaire to determine the impact of the illness on their daily life. Pictorial Bleeding Assessment Chart (PBAC): The history of the last menstruation period Participants will be asked to perform before starting the treatment : Complete blood count (CBC) Prothrombin Time (PT) Prothrombin ratio (INR) Fibrinogen (FIB) to detect bleeding disorders serum Creatinine to detect urinary toxicity
Masking
None (Open Label)
Allocation
N/A
Enrollment
13 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tea infusion
Arm Type
Experimental
Arm Description
The aerial parts of each plant were dried, then, they were powdered in a rotating knife grinder. The herbs were taken as tea infusion by the oral route. the powder of the mixture was added to 100 ml of boiling water and the tea infusion was taken three times a day for three consecutive days and it was repeated for three consecutive months
Intervention Type
Dietary Supplement
Intervention Name(s)
Tea infusion
Intervention Description
Herbal tea infusion will be administrated by the oral route before food
Primary Outcome Measure Information:
Title
Reduce the menstrual duration in days
Description
the Pictorial Blood Loss Assessment Chart (PBLAC) the number of bleeding day during menstruation
Time Frame
180 days
Title
Reduce the bleeding abundance
Description
bleeding abundance will be measured by the Pictorial Blood Loss Assessment Chart (PBLAC) The total score is calculated by adding up the sum of all scores for the sanitary pads used in the menstrual cycle. : 1 for lightly stained, 5 for moderately soiled, and 20 for completely saturated pads. Clots were given a score of 1 for small and 5 for large clots. Abnormal PBLAC bleeding score greater than or equal to 100, which correlates with bleeding abundance, defined as greater than 80 mL of menstrual blood loss. Normal bleeding is defined as a score of 75 or less. A score of 0 indicates amenorrhea or the absence of menstruation.
Time Frame
180 days
Secondary Outcome Measure Information:
Title
Change From Baseline in Hematocrit (Hct) Concentrations at Treatment Day 90
Description
Hematocrit was measured before treatment and after 90 days at the end of treatment
Time Frame
180 days
Title
Change From Baseline in Hemoglobin Concentration at Treatment Day 90
Description
Hemoglobin was measured before treatment and after 90 day A positive value indicates an increase in hemoglobin from baseline at treatment day 90
Time Frame
90 days
Title
Change From Baseline in Fibrinogen Concentration at Treatment Day 90
Description
Fibrinogen Concentration was measured before treatment and after 90 day
Time Frame
90 days
Title
Change From Baseline in Prothrombin Time at Treatment Day 90
Description
Prothrombin Time was measured before treatment and after 90 day
Time Frame
90 days
Title
hange From Baseline in serum Creatinine Time at Treatment Day 90
Description
to detect urinary toxicity. conducted at the start of the trial and after the last infusion consumption days 90
Time Frame
90 days

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Women suffering from AUB and being candidates for hysterectomy
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women failed first-line intervention to stop bleeding and planned for hysterectomy Women between (30-50 years) Able to understand and provide informed consent to participate in the study. Not pregnant or lactating Having menstrual period more than 7 days with uterine bleeding at irregular intervals. Exclusion Criteria: Participants with at least one of the following criteria will not be included in the trial: Chronic disease with long-term treatment (i.e. asthma, cardiovascular disorders..) woman taking any standard medications for abnormal uterine bleeding Women who have a history of gastrointestinal bleeding or ulcer Women who have abnormal kidney function Participants with increasing menstrual bleeding during the treatment requires surgical emergency procedures. Those refusing the instructions or participating in other clinical trials. Participant take other herbal treatment - Age less than 18 years - Healthy Volunteers women with ovarian tumours
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hedi Khairi, Pr
Organizational Affiliation
CHU, Farhat Hched Hospital, Faculty of medicine sousse tunisia 4000 Sousse Tunisia
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Latifa Lassoued, Pr.Ag
Organizational Affiliation
CHU Farhat Hached Hospital, Faculty of medicin Sousse,4000,Sousse,Tunisia
Official's Role
Study Director
Facility Information:
Facility Name
faculty of medicine Sousse
City
Sousse
ZIP/Postal Code
4000
Country
Tunisia

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
21666466
Citation
Donnez J, Squifflet J, Donnez O. Minimally invasive gynecologic procedures. Curr Opin Obstet Gynecol. 2011 Aug;23(4):289-95. doi: 10.1097/GCO.0b013e328348a283.
Results Reference
background
Citation
Bone, K., and Mills, S. Principles and practice of phytotherapy: Modern Herbal Medicine. Churchill Livingstone.2nd ed. Londo n: Elsevier. 2013; 9780702052972
Results Reference
background
PubMed Identifier
17218234
Citation
Istre O, Langebrekke A, Qvigstad E. Changing hysterectomy technique from open abdominal to laparoscopic: new trend in Oslo, Norway. J Minim Invasive Gynecol. 2007 Jan-Feb;14(1):74-7. doi: 10.1016/j.jmig.2006.08.011.
Results Reference
background
PubMed Identifier
19579942
Citation
Jazani NH, Ghasemnejad-Berenji H, Sadegpoor S. Antibacterial effects of Iranian Mentha pulegium essential oil on isolates of Klebsiella sp. Pak J Biol Sci. 2009 Jan 15;12(2):183-5. doi: 10.3923/pjbs.2009.183.185.
Results Reference
background
Citation
Kowalski R, Wawrzykowski J, Zawiślak G.Analysis of essential oils and extracts from Artemisia abrotanum L. and Artemisia dracunculus L. Herba Pol.2007.53: 246-254.
Results Reference
background
Citation
Teri Moser Woo, Marylou Robinson.Pharmaco therapeutics for Advance Practice Nurse Prescribers. Library of Congress. (2016:138-1520.
Results Reference
background
Citation
European Tea Committee (ETC), European Herbal Infusions Association (EHIA).Inventory List of Herbals Considered as Food. 2016 Available at: https://thie-online.eu/files/thie/docs/2019-09-26_PU_THIE_Inventory_List_status_27-06-2019_final.pdf
Results Reference
background
PubMed Identifier
20397217
Citation
Sutour S, Bradesi P, Casanova J, Tomi F. Composition and chemical variability of Mentha suaveolens ssp. suaveolens and M. suaveolens ssp. insularis from Corsica. Chem Biodivers. 2010 Apr;7(4):1002-8. doi: 10.1002/cbdv.200900365.
Results Reference
background
PubMed Identifier
17204526
Citation
Fraser IS, Critchley HO, Munro MG, Broder M. Can we achieve international agreement on terminologies and definitions used to describe abnormalities of menstrual bleeding? Hum Reprod. 2007 Mar;22(3):635-43. doi: 10.1093/humrep/del478. Epub 2007 Jan 4.
Results Reference
background
Citation
Oueslati, S, Karray-Bouraoui, N, Attia, H. et al. Physiological and antioxidant responses of Mentha pulegium (Pennyroyal) to salt stress. Acta Physiol Plant 32. 2010.289-296. https://doi.org/10.1007/s11738-009-0406-0
Results Reference
background
Citation
Chopra, R.N, Nayar S.L, Chopra, I.C. Glossary of Indian Medicinal Plant, New Delhi. CSIR.1956 .1-330.
Results Reference
background
PubMed Identifier
25268434
Citation
Hoffmann TC, Montori VM, Del Mar C. The connection between evidence-based medicine and shared decision making. JAMA. 2014 Oct 1;312(13):1295-6. doi: 10.1001/jama.2014.10186. No abstract available.
Results Reference
background
PubMed Identifier
24888316
Citation
Qaraaty M, Kamali SH, Dabaghian FH, Zafarghandi N, Mokaberinejad R, Mobli M, Amin G, Naseri M, Kamalinejad M, Amin M, Ghaseminejad A, HosseiniKhabiri SJ, Talei D. Effect of myrtle fruit syrup on abnormal uterine bleeding: a randomized double-blind, placebo-controlled pilot study. Daru. 2014 Jun 2;22(1):45. doi: 10.1186/2008-2231-22-45.
Results Reference
background
PubMed Identifier
18345348
Citation
Kang M, Ragan BG, Park JH. Issues in outcomes research: an overview of randomization techniques for clinical trials. J Athl Train. 2008 Apr-Jun;43(2):215-21. doi: 10.4085/1062-6050-43.2.215.
Results Reference
background

Learn more about this trial

Therapeutic Effect of Herbal Infusion on Menometrorrhagia

We'll reach out to this number within 24 hrs