Dose Comparison of Misoprostol for Cervix Ripening Before Operative Hysteroscopy.

Cervix; Open Clinical Trial

Official title:

Comparison Between 200 μg and 800 μg of Misoprostol for Cervical Ripening Prior to Operative Hysteroscopy: Randomized and Quadruple Blind Clinical Trial.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04152317
• Other study ID #: MISO.
• Status: Completed
• Phase: Phase 3
• Start date: November 7, 2019
• Est. completion date: September 12, 2020

Study information

• Verified date: October 2020
• Source: Professor Fernando Figueira Integral Medicine Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The medication misoprostol is used to facilitate the entry into the uterus of hysteroscopy surgery equipment and this research aims to compare the results of the use of this drug in two different doses trying to find the optimal one.

To perform this work we will use the misoprostol and will perform a questionnaire that will be asked during hospitalization, before, during and the 12hours after the surgery.

The patients who meet the inclusion criteria after signing the Informed Consent Form will be allocated into two groups getting misoprostol 200mcg or misoprostol 800mcg.

Description:

Background: Hysteroscopy represents a minimally invasive procedure that has been increasing its adoption in the treatment of many cervical canal and uterine cavity disorders. However, difficulties related to the introduction of the equipment through the cervix are frequent. Although several studies suggest advantages in the cervical preparation with misoprostol, reducing the resistance of the uterine cervix, systematic reviews are unison to indicate the need for clarification on the ideal dose.

Aim: Compare the intra and postoperative results of patients submitted to cervical dilatation for surgical hysteroscopy with previous use of misoprostol at doses of 200mcg or 800mcg for uterine cervix preparation at Recife school hospitals.

Methods: Randomized, quadruple-blind clinical trial with patients who underwent cervical dilatation prior to surgical hysteroscopy at Recife school hospitals, Pernambuco. Patients included will be allocated randomly into two groups. The first group will use misoprostol in the dosage of 200mcg and the second, will use the dosage of 800mcg. Administration, via the vaginal route, will occur 12 hours before performing the operative hysteroscopy. The following variables will be studied: cervical canal width, cervical length, degree of difficulty, duration and failure of cervical dilation, side effects, surgical complications and patient's satisfaction. For statistical analysis, chi-square tests of association, Fisher's exact and Mann-Whitney tests will be used to compare the groups, with an alpha error of less than 5% being considered significant.

Ethical aspects: This study will comply with Resolution 466/12 of the National Health Council and was submitted to and approved by the Professor Fernando Figueira Integral Medicine Institute Research Ethics Committee, beginning only after this approval. All participants will only be included if they voluntarily agree to participate by signing the Free and Informed Consent Form.

There are no conflicts of interest.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: September 12, 2020
• Est. primary completion date: September 11, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with indication for operative hysteroscopic.

Exclusion Criteria:

• Patient with contraindications to the use of prostaglandins such as asthma, glaucoma, renal failure, severe heart disease or drug allergy;

• Situations that impede the vaginal administration of medication such as major genital prolapse and virginity;

• Situations that prevent hysteroscopy as major uterine bleeding, diagnosis or suspected topical pregnancy and genital infection such as vaginosis and cervicitis;

• Situations that may influence cervical canal width such as a history of isthmo-cervical incompetence or major cervical surgery like conization or trachelotomy; presence of any structure like uterine fibroid or endometrial polyp inside the cervical canal or though the cervical os; patients on systemic or vaginal estrogen replacement therapy or who have recently used gonadotropin hormone-releasing hormone analogues.

Related Conditions & MeSH terms

• Cervix; Open
• Uterine Cervical Incompetence

Intervention

Drug:
• Misoprostol 200mcg Tab
In the misoprostol 200mcg group there will be one tablet of 200mcg and three identical tablets in shape, size and color without pharmacological properties. These four tablets will be single dose administered via vaginal route for each participant.
• Misoprostol 800mcg Tab
In the misoprostol 800mcg group there will be four tablets of 200mcg. These four tablets will be single dose administered via vaginal route for each participant.

Locations

Country	Name	City	State
Brazil	Maria da Conceição Souto Maior	Recife	PE

Sponsors (1)

Lead Sponsor	Collaborator
Professor Fernando Figueira Integral Medicine Institute

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cervical canal width.	Maximum size of dilator that passes through the internal os without resistance.	during the surgery
Secondary	Time required to dilate the cervix to 9mm.	Time necessary to achieve cervical permeability up to 9mm by introducting the Hegar dilators through the internal os.	during the surgery
Secondary	Ease of cervical dilation.	The feeling of ease or difficulty reported by the surgeon while dilating the cervix.; Evaluated by LIKERT scale. It varies from one to five, one meaning very difficult and five meaning very easy .	during the surgery
Secondary	Length of the cervix.	The distance between the external and the internal os measured in centimeters.	during the surgery
Secondary	Abandonment of the procedure due to cervical dilation failure.	Impossibility of perform operative hysteroscopy due to difficulty to achieve complete cervical dilation up to 9mm.	during the surgery
Secondary	Intraoperative complications.	Complications related to the difficulty of the dilate de cervical canal like uterine perforation, creation of false path, cervical tears and post-dilation bleeding.	during the surgery
Secondary	Side effects due to the use of the misoprostol.	Adverse effects as nausea, vomiting, diarrhea, fever, chills, abdominal pain or any other complaint resulting from the use of the medication.	24 hours
Secondary	Pain intensity	The highest level of pain reported by the patient according the Visual Analog Scale evaluated at 3 moments: at the time of hospitalization, at the preoperative time (between medication administration and anesthesia onset) and at the postoperative time (12 hours after the procedure).	24 hours
Secondary	Patient satisfaction degree.	The satisfaction with the medication, reported by the participant. Evaluated by LIKERT scale. It varies from one to five, one meaning less than satisfied and five meaning very satisfied with the drug.	24 hours