ClinicalTrials.gg
Status unknownNCT01634633Updated Jul 6, 2012

Endometrial Nerve Fibers Detection in Patients With Different Gynecological Pathologies

An observational study in Gynecological Pathologies, sponsored by Ain Shams Maternity Hospital. Status unknown at 1 site in Egypt. Open to female participants aged 20 Years to 60 Years. Per ClinicalTrials.gov, last updated 2012-07-06.

Sponsored by Ain Shams Maternity Hospital · Observational

The sponsor has not verified this record recently (last verified Jul 2012), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Time perspective
Cross-sectional
Enrollment
300
Ages
20 Years to 60 Years
Sex
Female
01

Study summary

The aim of this study is to investigate the prevelence of endometrial nerve fibers in different gynecological pathologies

Read the detailed description

The aim of this study is to investigate the prevelence of endometrial nerve fibers in different gynecological pathologies in addition to its relation to chronic pelvic pain

02

Conditions studied

  • Gynecological Pathologies

Keywords

  • Endometrial nerve fibres
03

In context

Lead sponsor

Ain Shams Maternity Hospital is the lead sponsor of 139 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 60 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

The population of this study will be 300 patient undergoing laparoscopy or laparotomy for different gynecological diseases namely, polycystic ovarian disease (PCOD), ovarian cysts either benign or malignant, fibroid uterus, adenomyosis, endometrial hyperplasia and endometrial carcinoma

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Age: 20-60 years of age.
  2. Written and signed informed consent by the patient to participate in the study.
  3. Women candidate for surgical intervention either via laparoscopy or laparotomy for different gynecological pathologies

Exclusion criteria

Exclusion Criteria:

  1. Suspected endometriosis.
  2. Patient unwillingness to participate in the study.
  3. No hormonal treatment for the last 6 months.
  4. Suspected pregnancy.
05

Study design

Time perspective
Cross-sectional
Enrollment
300 participants (estimated)
06

What researchers measure

Primary outcomes

  1. Prevelencce of endometrial nerve fibers

    Is to determine the prevelence of endometrial nerve fibers in different gynecological pathologies I via endometrial sampling

    Time frame: 18 months

Secondary outcomes

  1. Pelvic pain

    Relating the density of endometrial nerve fibres to different types of pelvic pain

    Time frame: 18 months

07

Study locations

1 of 1 sites recruiting
  • Ain shams new maternity hospital
    Cairo, 11591, Egypt
    • Reda MK Ghanem, MD · Principal investigator
    • Reda MK Ghanem, M.B.B.Ch · Principal investigator
    Recruiting
08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jan 2011, a primary completion of Nov 2012 and a completion of Dec 2012. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 3, 2012
First posted
Jul 6, 2012
Start
Jan 2011
Primary completionEst.
Nov 2012
CompletionEst.
Dec 2012
Last update
Jul 6, 2012
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 6, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01634633
Responsible party
reda mokhtar kamal ghanem (Mr, Ain Shams University) — Principal investigator
First posted
Jul 6, 2012
Start date
Jan 2011
Primary completion
Nov 2012 (estimated)
Completion
Dec 2012 (estimated)
Last update
Jul 6, 2012

Study contacts

Ahmed EH Elbohoty, MD
Contact
elbohoty79@yahoo.com
22590767 ext. 00202
Karim HI Abd-El-Maeboud, MD
Contact
kabdelmaeboud@yahoo. com
24140680 ext. +202
Reda MK Ghanem, M.B.B.Ch
principal investigator · Ain Shams University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2012. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion