Labor ComplicationlabourRecordNCT03272282
Paperless Parotograph in Evaluation of Labour
An observational study of Labor Complication, run by Assiut University at 2 sites in Egypt.
Trial summary
Using Paperless partograph management of labour as simple tool to prevent obstructed labour or prolonged labour or its complications at the mother or her fetus Read more about this study
- Who is it for?
- Ages 20 to 42 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Labor Complication
- How many people
- 450 participants
- Where
- 2 sitesEgypt
- Study dates
- 12 Jan 2017to 12 Sep 2017
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 20 to 42 years
- Women only
- Healthy volunteers accepted
- Adult
Study population: By following women during labour using well structured questions developed by researcher and filling well designed Paperless partograph stumped THE collected data will be analysed using special computer program SPSS tactical program for social science
Who may be able to join
- women ln active phase of labour
- With single pregnanncy
- living fetus
- cephalic presentation
- occipt anterior
- 36 weak gestional age up to full term
Who cannot join
- preterm . .or women with antipartum hemorrhage .
- or multipregnanncy
- previous utrine surgery
- or abnormal cardiotocograph(CTG )PATTERN
- or any heart disease of mother or his fetus
Trial locations and contacts
2 sites in 1 country.
Egypt2 sites, 2 recruiting
- Recruiting
Faculity of Medicine Assiut University
Asyut, Asyut Governorate, 71723
abo baker, pro, 00201003568474, kotbnetw@hotmail.com
said mostafa, pro, 00201007599819, saidmostafy9@gmail.com
- Recruiting
Faculity of Medicine
Asyut, 71723
abobaker khalil abass metwally, professor, 002010033568474, kotbnetw@hotmail.com
said mohamed mostafy, profossor, 00201007599819, saidmostafy9@gmail.com
About this study
Official title: Paperless Partograph Evaluation of Labour
Using Paperless partograph management of labour as simple tool to prevent obstructed labour or prolonged labour or its complications at the mother or her fetus
Read the detailed description
WHO PARTOGRAPH is very work load need more time and more stuff in both treaning and learning for plotting and for drowning but inside labour room needing simple partograph playing the simple partograph beast role in management of labour and stand test against time for saving live of labour women and her child Paperless parotograph can help obestitricianes to talk decision about when to transferr the labourus women to higher centers on to make medical intervention or what time to end labour by caesarian section
- Conditions
- Labor Complication
- Keywords
- WHO PARTOGRAPG.OBSTRUCTED LABOUR. managment of labour
- Medical subject headings
- Obstetric Labor Complications
What is being measured
The primary outcome is the main question the study is designed to answer.
Progress of labour
Cervical dilatation 1 cm / hour
Measured: up to 5 months
Secondary outcomes (2)
Charcteristics of new_born
Apgar score at1minute and Apgar score at 5minutes
Measured: up to 1 month
Time taken after ALERT EDT
Primgravida and Multipara
Measured: up to 2 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Sep 2017
- Study start12 Jan 2017
- Primary completion12 Sep 2017 (estimated)
- Study completion12 Sep 2017 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for Labor ComplicationStudies of the same condition, open and under way.
- More trials run by Assiut UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case crossover
- Time perspective
- Prospective
- Enrolment
- 450 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Assiut University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, ayman darder, Assiut University
- Investigators
- mohamed khalaph, Study director, assiut universty faculity of medicineahmad abass, Study chair, assiut university faclity of meficibe
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03272282
- Sponsor's protocol ID
- paperlesspartograph
- Acronym
- labourRecord
- Status last verified
- Sep 2017
- First submitted
- 23 Aug 2017
- Last updated
- 6 Sep 2017
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Fatehi F, Gray LC, Wootton R. How to improve your PubMed/MEDLINE searches: 3. advanced searching, MeSH and My NCBI. J Telemed Telecare. 2014 Mar;20(2):102-12. doi: 10.1177/1357633X13519036.
PubMed 24614997Jadad AR, McQuay HJ. Searching the literature. Be systematic in your searching. BMJ. 1993 Jul 3;307(6895):66. doi: 10.1136/bmj.307.6895.66-a. No abstract available.
PubMed 8343701Chang AA, Heskett KM, Davidson TM. Searching the literature using medical subject headings versus text word with PubMed. Laryngoscope. 2006 Feb;116(2):336-40. doi: 10.1097/01.mlg.0000195371.72887.a2.
PubMed 16467730
Study at a glance
From the registry record, last updated by the sponsor on 6 Sep 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Paperless Partograph Evaluation of Labour
- ClinicalTrials.gov ID
- NCT03272282
- Acronym / sponsor ID
- labourRecord / paperlesspartograph
- Conditions
- Labor Complication
- Keywords
- WHO PARTOGRAPG.OBSTRUCTED LABOUR. managment of labour
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 450 participants (estimated)
- Lead sponsor
- Assiut UniversityUniversity, hospital or other
- Study start
- 12 Jan 2017 (actual)
- Primary completion
- 12 Sep 2017 (estimated)
- Study completion
- 12 Sep 2017 (estimated)
- First posted
- 5 Sep 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Using Paperless partograph management of labour as simple tool to prevent obstructed labour or prolonged labour or its complications at the mother or her fetus
Detailed description
WHO PARTOGRAPH is very work load need more time and more stuff in both treaning and learning for plotting and for drowning but inside labour room needing simple partograph playing the simple partograph beast role in management of labour and stand test against time for saving live of labour women and her child Paperless parotograph can help obestitricianes to talk decision about when to transferr the labourus women to higher centers on to make medical intervention or what time to end labour by caesarian section
Study design
- Observational model
- Case crossover
- Time perspective
- Prospective
Who may qualify
- Ages
- 20 to 42 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- By following women during labour using well structured questions developed by researcher and filling well designed Paperless partograph stumped THE collected data will be analysed using special computer program SPSS tactical program for social science
Key inclusion criteria (6 listed)
- women ln active phase of labour
- With single pregnanncy
- living fetus
- cephalic presentation
- occipt anterior
Key exclusion criteria (5 listed)
- preterm . .or women with antipartum hemorrhage .
- or multipregnanncy
- previous utrine surgery
- or abnormal cardiotocograph(CTG )PATTERN
- or any heart disease of mother or his fetus
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Progress of labour
Time frame: up to 5 months
Cervical dilatation 1 cm / hour
2 secondary outcomes
Charcteristics of new_born
Time frame: up to 1 month
Time taken after ALERT EDT
Time frame: up to 2 months
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Sep 2017.
- Results publication: PubMed 24614997Fatehi F, Gray LC, Wootton R. How to improve your PubMed/MEDLINE searches: 3. advanced searching, MeSH and My NCBI. J Telemed Telecare. 2014 Mar;20(2):102-12. doi: 10.1177/1357633X13519036.
- Results publication: PubMed 8343701Jadad AR, McQuay HJ. Searching the literature. Be systematic in your searching. BMJ. 1993 Jul 3;307(6895):66. doi: 10.1136/bmj.307.6895.66-a. No abstract available.
- Results publication: PubMed 16467730Chang AA, Heskett KM, Davidson TM. Searching the literature using medical subject headings versus text word with PubMed. Laryngoscope. 2006 Feb;116(2):336-40. doi: 10.1097/01.mlg.0000195371.72887.a2.
- more information can present in thishomepageLink provided by the sponsor.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
mohamed khalaph study director
assiut universty faculity of medicine
ahmad abass study chair
assiut university faclity of meficibe
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Labor Complication, run by Assiut University at 2 sites in Egypt.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 6 Sep 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact abobaker khalil (00201003568474, kotbnetw@hotmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Progress of labour (time frame: up to 5 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03272282, which also lists 3 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Sep 2017.