Hysterectomy Clinical Trial
— HERBALTREATOfficial title:
The Therapeutic Effect of Traditional Herbal Tea Infusion on Abnormal Uterine Bleeding- Menometrorrhagia
NCT number | NCT05406960 |
Other study ID # | FMSELMI |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | May 10, 2019 |
Est. completion date | February 10, 2021 |
Verified date | June 2022 |
Source | Faculty of Medicine, Sousse |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 13 |
Est. completion date | February 10, 2021 |
Est. primary completion date | December 20, 2020 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 30 Years to 55 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
Tunisia | faculty of medicine Sousse | Sousse |
Lead Sponsor | Collaborator |
---|---|
Faculty of Medicine, Sousse | Centre Hôpital Universitaire Farhat Hached |
Tunisia,
Bone, K., and Mills, S. Principles and practice of phytotherapy: Modern Herbal Medicine. Churchill Livingstone.2nd ed. Londo n: Elsevier. 2013; 9780702052972
Chopra, R.N, Nayar S.L, Chopra, I.C. Glossary of Indian Medicinal Plant, New Delhi. CSIR.1956 .1-330.
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. Review. — View 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
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. Epub 2007 Jan 4. — View 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. — View 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. — View 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. — View 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. — View Citation
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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
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;22:45. doi: 10.1186/2008-2231-22-45. — View Citation
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Reduce the menstrual duration in days | the Pictorial Blood Loss Assessment Chart (PBLAC) the number of bleeding day during menstruation | 180 days | |
Primary | 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. |
180 days | |
Secondary | 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 | 180 days | |
Secondary | 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 | 90 days | |
Secondary | Change From Baseline in Fibrinogen Concentration at Treatment Day 90 | Fibrinogen Concentration was measured before treatment and after 90 day | 90 days | |
Secondary | Change From Baseline in Prothrombin Time at Treatment Day 90 | Prothrombin Time was measured before treatment and after 90 day | 90 days | |
Secondary | 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 | 90 days |
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