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Paracervical Block Versus Transcervical Block in Outpatient Procedural Hysteroscopy

Primary Purpose

Myoma;Uterus, Polyp Uterus

Status
Not yet recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Bupivacaine Injection
Sponsored by
Ciusss de L'Est de l'Île de Montréal
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Myoma;Uterus focused on measuring hysteroscopy, pain, local anesthetic, ambulatory care, bupivacaine, paracervical block, transcervical block

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Female patients 18 years of age or older Indication of outpatient surgical hysteroscopy for polypectomy and myomectomy Exclusion Criteria: Women under 18 years old Unable to understand how to score a visual analog scale pain score Hysteroscopy contraindication Patients with medical history or current status that makes outpatient procedure usafe

Sites / Locations

  • CIUSSS de l'Est de l'Île de Montréal

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Paracervical block

Transcervical block

Arm Description

10cc Bupivacaine 1% at 0.5-1 cm depth of the cervicovaginal junction at 5 and 7 o'clock positions (20cc in total).

10cc Bupivacaine 1% through the endocervix using an 17-gauge epidural catheter

Outcomes

Primary Outcome Measures

To assess the best anesthetic pathway to decrease pain during outpatient hysteroscopy
comparing 10 point visual analogue scale (from 0 to 10 points) between two groups of patients recieving Bupivacaine administrated through a paracervical block versus a transcervical block
To assess the best anesthetic pathway to decrease pain during outpatient hysteroscopy
comparing 10 point visual analogue scale (from 0 to 10 points) between two groups of patients recieving Bupivacaine administrated through a paracervical block versus a transcervical block

Secondary Outcome Measures

Compare the pain experience based on the visual analogue scale between pre and post-menopausal patients
Compare the pain experience based on the 10 point visual analogue scale (from 0 to 10 points) between pre and post-menopausal patients
Compare the pain experience based on the visual analogue scale between pre and post-menopausal patients
Compare the pain experience based on the 10 point visual analogue scale (from 0 to 10 points) between pre and post-menopausal patients
Compare the pain experience based on the visual analogue scale between nulliparous and parous patients
Compare the pain experience based on the 10 point visual analogue scale (from 0 to 10 points) between nulliparous and parous patients
Compare the pain experience based on the visual analogue scale between nulliparous and parous patients
Compare the pain experience based on the 10 point visual analogue scale (from 0 to 10 points) between nulliparous and parous patients
To evaluate the need for an extra intravenous sedative dose.
Number of patients who demand an extra dose of sedative during hysteroscopy

Full Information

First Posted
June 19, 2023
Last Updated
July 20, 2023
Sponsor
Ciusss de L'Est de l'Île de Montréal
Collaborators
Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal
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1. Study Identification

Unique Protocol Identification Number
NCT05967936
Brief Title
Paracervical Block Versus Transcervical Block in Outpatient Procedural Hysteroscopy
Official Title
A Prospective Randomized Study Comparing Different Types of Local Anesthesia in Outpatient Procedural Hysteroscopy
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 1, 2023 (Anticipated)
Primary Completion Date
September 1, 2024 (Anticipated)
Study Completion Date
December 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ciusss de L'Est de l'Île de Montréal
Collaborators
Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal

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
No

5. Study Description

Brief Summary
Hysteroscopy is a minimally invasive, diagnostic and therapeutic gynecological surgical technique and the gold standard in the study of the uterine cavity. Thanks to the decrease in the diameter of hysteroscopes and to the vaginoscopic approach, anesthesia is no longer necessary in diagnostic hysteroscopy. Nevertheless, in operative hysteroscopy, given the instrumentalization and the need of cervical dilation, the use of local anesthesia, with or without sedation, is recommended. The different alternatives described in the literature are the following: Cervical/ intracervical block: injection of local anesthetic into the four quadrants of the cervix. Paracervical block: injection of local anesthetic in the cervicovaginal junction at 5 and 7 o'clock positions. Transcervical (uterine) anesthesia: instillation of a local anesthetic agent via catheter through the cervix and into the uterine cavity. Topical cervical anesthesia: application of local anesthetic in gel or spray to the cervix. To assess the best anesthetic pathway to decrease pain during outpatient hysteroscopy, the investigators will perform a prospective multicentric study that compare two types of local anesthesia in outpatient procedural hysteroscopy: paracervical block, that is the actual gold-standard, and transcervical instillation.
Detailed Description
To assess the best anesthetic pathway to decrease pain during outpatient hysteroscopy, the investigators will perform a multicentric prospective randomized trial, single-blinded, that compares two types of local anesthesia in outpatient procedural hysteroscopy: paracervical block, that is the actual gold-standard, and transcervical instillation. The population studied will consist in adult women with indication of an outpatient surgical hysteroscopy (myomectomy or polypectomy). Every one of them will be invited to participate the day of their procedure. In the outpatient hysteroscopy clinic, the investigators will verify inclusion and exclusion criteria, explain the objectives of the study, collect data and obtain the patient's consent. The sample size is 242 patients (121 in each group). The study will be performed in two different centers: Integrated University Health Center and Social Services of the East of the Island of Montreal Integrated University Health Center and social services of the South Center of the Island of Montreal Right before each procedure the patients will be randomized through anonymous and alternized enveloppes that will be distributed in each center, to either receive paracervical or transcervical anesthesia before hysteroscopy. Each patient will receive a pre-established dose of sedative before the procedure, according to their weight: Fentanyl 0,5 mcg/kg IV and Midazolam 0,02 mg/kg. The subsequent doses will be noted. Under sedation, with the patient in lithotomy position, a medium size speculum will be inserted. The vagina will be disinfected with chlorhexidine and the anterior lip of the cervix will be gripped with a Pozzi forceps. According to previous randomization, each patient will receive one of the following alternatives of local anesthesia: Group A: Paracervical 10cc Bupivacaine 1%, without epinephrine, at 0.5-1 cm depth of the cervicovaginal junction at 5 and 7 o'clock positions (20cc in total). Group B: Transcervical (uterine) 10cc Bupivacaine 1% through the endocervix using an 17-Gauge epidural catheter During the procedure (T1), the nurse will be in charge to fill the scale (to avoid bias). The patients will be given a Visual Analogue Scale (VAS) to fill 15 minutes after the procedure (before discharge), to assess pain. For each group the investigators will calculate the average rate of pain according to the Visual Analogue Scale during and immediately after the procedure (15 minutes). The investigators will subdivide each group into pre and postmenopausal women and into nulliparous and parous women and compare their Visual Analogue Scale as well. Statistical analysis will be performed to compare results.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myoma;Uterus, Polyp Uterus
Keywords
hysteroscopy, pain, local anesthetic, ambulatory care, bupivacaine, paracervical block, transcervical block

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Multicentric, prospective, randomized trial, single-blinded, where eligible patients will be randomized to either receive paracervical or transcervical anesthesia before outpatient surgical hysteroscopy
Masking
Participant
Allocation
Randomized
Enrollment
242 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Paracervical block
Arm Type
Active Comparator
Arm Description
10cc Bupivacaine 1% at 0.5-1 cm depth of the cervicovaginal junction at 5 and 7 o'clock positions (20cc in total).
Arm Title
Transcervical block
Arm Type
Experimental
Arm Description
10cc Bupivacaine 1% through the endocervix using an 17-gauge epidural catheter
Intervention Type
Drug
Intervention Name(s)
Bupivacaine Injection
Other Intervention Name(s)
evaluation of pain by using two different types of local anesthesia
Intervention Description
evaluation of pain by using two different types of local anesthesia
Primary Outcome Measure Information:
Title
To assess the best anesthetic pathway to decrease pain during outpatient hysteroscopy
Description
comparing 10 point visual analogue scale (from 0 to 10 points) between two groups of patients recieving Bupivacaine administrated through a paracervical block versus a transcervical block
Time Frame
during hysteroscopy
Title
To assess the best anesthetic pathway to decrease pain during outpatient hysteroscopy
Description
comparing 10 point visual analogue scale (from 0 to 10 points) between two groups of patients recieving Bupivacaine administrated through a paracervical block versus a transcervical block
Time Frame
15 minutes post hysteroscopy
Secondary Outcome Measure Information:
Title
Compare the pain experience based on the visual analogue scale between pre and post-menopausal patients
Description
Compare the pain experience based on the 10 point visual analogue scale (from 0 to 10 points) between pre and post-menopausal patients
Time Frame
during hysteroscopy
Title
Compare the pain experience based on the visual analogue scale between pre and post-menopausal patients
Description
Compare the pain experience based on the 10 point visual analogue scale (from 0 to 10 points) between pre and post-menopausal patients
Time Frame
15 minutes post hysteroscopy
Title
Compare the pain experience based on the visual analogue scale between nulliparous and parous patients
Description
Compare the pain experience based on the 10 point visual analogue scale (from 0 to 10 points) between nulliparous and parous patients
Time Frame
during hysteroscopy
Title
Compare the pain experience based on the visual analogue scale between nulliparous and parous patients
Description
Compare the pain experience based on the 10 point visual analogue scale (from 0 to 10 points) between nulliparous and parous patients
Time Frame
15 minutes post hysteroscopy
Title
To evaluate the need for an extra intravenous sedative dose.
Description
Number of patients who demand an extra dose of sedative during hysteroscopy
Time Frame
during hysteroscopy

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Female patients 18 years of age or older Indication of outpatient surgical hysteroscopy for polypectomy and myomectomy Exclusion Criteria: Women under 18 years old Unable to understand how to score a visual analog scale pain score Hysteroscopy contraindication Patients with medical history or current status that makes outpatient procedure usafe
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Janey Fang, MD
Phone
5142513051
Email
jfang85@uwo.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Chantal Rivard, MD
Phone
5142513051
Email
rivardch@videotron.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mélissa Roy, MD
Organizational Affiliation
OB-GYN
Official's Role
Study Director
Facility Information:
Facility Name
CIUSSS de l'Est de l'Île de Montréal
City
Montréal-Est
State/Province
Quebec
ZIP/Postal Code
H1T 2M4
Country
Canada
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Janey Fang, MD
Phone
5142513051
Email
jfang85@uwo.ca
First Name & Middle Initial & Last Name & Degree
Chantal Rivard, MD
Phone
5142513051
Email
rivardch@videotron.ca
First Name & Middle Initial & Last Name & Degree
Paz Garcia, MD
First Name & Middle Initial & Last Name & Degree
Mélissa Roy, MD
First Name & Middle Initial & Last Name & Degree
Janey Fang, MD
First Name & Middle Initial & Last Name & Degree
Chantal Rivard, MD
First Name & Middle Initial & Last Name & Degree
Émilie Hudon, MD
First Name & Middle Initial & Last Name & Degree
Émilie Gorak, MD
First Name & Middle Initial & Last Name & Degree
Mik Gangal, MD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is not a plan to make IPD available
Citations:
PubMed Identifier
15559340
Citation
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Results Reference
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Citation
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Results Reference
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PubMed Identifier
31982584
Citation
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Results Reference
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PubMed Identifier
9050737
Citation
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PubMed Identifier
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Citation
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PubMed Identifier
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Citation
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Paracervical Block Versus Transcervical Block in Outpatient Procedural Hysteroscopy

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