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What Amount of Stress is Enough for a Successful Conception?

Impact of Premedication With Midazolam in Aspiration Procedures On Stress Levels During IVF Procedures

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04160611
Enrollment
40
Registered
2019-11-13
Start date
2019-09-01
Completion date
2020-10-01
Last updated
2019-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

In Vitro Fertilization, Midazolam Adverse Reaction, Stress, Stress, Emotional

Keywords

IVF, stress, midazolam, premedication

Brief summary

The aim of the study is to determine whether premedication with midazolam before oocyte aspiration in IVF procedures affects the amount of (oxidative) stress in women undergoing IVF and whether stress is also transmitted to the follicular fluid of aspirated follicles. The primary endpoint is the impact of stress during aspiration on the success of medically assisted fertilization (IVF / ICSI in the stimulated cycle).

Detailed description

The procedure of in vitro fertilisation (IVF) is used to treat the infertility problems. The procedure includes ovary aspiration, to isolate oocytes. During the aspiration the patient is sedated with short-term intravenous aesthetic. Premedication is often used in anaesthesiology, and includes drugs application 30 minutes prior to procedure to sedate and treat the anxieties of the patient. One of the most often used drugs in premedication is midazolam. As the procedure is quite stressful for the patients, our aim is to investigate the influence of midazolam premedication on the stress release during the oocyte aspiration procedure, as well as its influence on the whole IVF procedure. Therefore, patients will be divided into two groups, control and midazolam. Blood samples will be taken before and during the procedure. Stress, antioxidant parameters (with glutathione and catalase) and oxidative status will be monitored in serum and follicular fluid. The results will be correlated with subjective stress levels in the two groups in an effort to establish ties with IVF results.

Interventions

DRUGMidazolam 7.5mg

The patient groups differ only in that respect that the intervention group will receive oral midazolam 7.5 g before oocyte aspiration.

Sponsors

University Hospital Sestre Milosrdnice
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Two randomized groups receiving midazolam/not receiving midazolam premedication before oocyte aspiration procedures as part of IVF procedures

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Informed consent, healthy women undergoing IVF procedures for the first time

Exclusion criteria

* Refusal to enroll, chronic endocrine and psychiatric illnesses that might affect baseline stress levels

Design outcomes

Primary

MeasureTime frameDescription
Stress Levels in Premedicated Women3 hours post-surgeryAll patients in the midazolam group will be sampled with 5 ml venepuncture prior to midazolam administration, just before the procedure, 2 hours after the procedure. A follicular fluid sample will be taken at the procedure. Samples will be stored in the freezer at -80⁰C. The total antioxidant capacity (TAC) and total oxidation capacity (TOC) of commercially available kits will be determined from plasma and follicular fluid. Whole blood will determine total glutathione and catalase activity. In addition to the total oxidation capacity, the amount of HNE-protein conjugates will be determined from the follicular fluid as an indicator of lipid peroxidation, and the Patients will be monitored after the aspiration procedure, and the success of the procedure of medically assisted fertilization, ie number of pregnancies, in the test and control group will be monitored.

Countries

Croatia

Contacts

Primary ContactAndro Košec, MD, PhD
andro.kosec@yahoo.com+385989817156
Backup ContactMaja Pešić, MD
majapesic1980@gmail.com+385989817156

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026