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Effect of Fentanyl on Main Opioid Receptor (OPRM1) on Human Granulosa Cells.

Effect of Fentanyl on Expression of Main Opioid Receptor (OPRM1) on Human Granulosa Cells During Ultrasound-guided Transvaginal Oocyte Retrieval.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03248076
Enrollment
30
Registered
2017-08-14
Start date
2017-04-01
Completion date
2018-10-10
Last updated
2017-12-14

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

Conditions

Opioid Use, Stress Reaction

Brief summary

Opioids is known that produce not only analgesia but also hyperalgesia through activation of central glutaminergic system-GABA. At the same time, recently it was found that the main opioid receptor (OPRM1) is present on human granulosa cells and exogenous opiates and their antagonists can influence granulosa cell vascular endothelial growth factor (VEGF) production via OPRM1, causing ovarian hyperstimulation syndrome. This study aims to investigate if a single exposure to opioids is enough to produce activation of stress mechanism during oocyte retrieval.

Detailed description

The main opioid receptor (OPRM1) is present on human granulosa cells and exogenous opiates and their antagonists can influence granulosa cell vascular endothelial growth factor (VEGF) production via OPRM1, causing ovarian hyperstimulation syndrome. This study aims to investigate if a single exposure to opioids is enough to produce activation of stress mechanism during ultrasound-guided oocyte retrieval. It will be measured the level of cortisone before and 15min after iv administration of fentanyl on blood and on oocyte fluid.

Interventions

DRUGFentanyl Citrate

1γ/Kg fentanyl

Sponsors

Papanikolaou Evaggelos
CollaboratorUNKNOWN
Naidecki Robert
CollaboratorUNKNOWN
Pakaki Fay
CollaboratorUNKNOWN
Raikos Nikolaos
CollaboratorUNKNOWN
George Papanicolaou Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 32 Years
Healthy volunteers
Yes

Inclusion criteria

* American Physical Status I-III, BMI\<30,

Exclusion criteria

* Heart failure * hepatic failure, hepatitis, * drug abuse * receiving b blockers * receiving b agonists (even bronchodilators)

Design outcomes

Primary

MeasureTime frameDescription
fentanyl15 minutesfentanyl on blood sample and oocyte fluid

Secondary

MeasureTime frameDescription
cortisone15 mincortisone on blood sample and oocyte fluid

Countries

Greece

Contacts

Primary ContactIrene Asouhidou, MD, PhD
iasouh@aol.com00302310999321
Backup ContactEvaggelos Papanikolaou, MD, PhD
drvagpapanikolaou@yahoo.gr00302310424294

Outcome results

None listed

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