Obstructive Sleep ApneaNCT02016638
Sleep Quality in Pregnancy and Its Impact on Pregnancy Outcomes
A study testing Polysomnography and ambulatory blood pressure recording in people with Obstructive Sleep Apnea and Pregnancy Induced Hypertension, run by All India Institute of Medical Sciences at 1 site in India.
Trial summary
Hypothesis:Sleep Disorders are very common during pregnancy but the their exact role in causation of pregnancy related disorders is yet to be determined. OSA can complicate pregnancy given the risk factors of weight gain, upper displacement of the diaphragm, and hormonal-induced hyperaemia of the nasopharyngeal… Read more about this study
- Who is it for?
- Ages 20 to 45 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Obstructive Sleep Apnea, Pregnancy Induced Hypertension, High-Risk Pregnancy
- What is being tested?
- Polysomnography and ambulatory blood pressure recording
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 200 participants
- Where
- 1 siteIndia
- Study dates
- Mar 2013to May 2014
- Phase
- Interventional
- 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 45 years
- Women only
- Healthy volunteers accepted
- Adult
Who may be able to join
- Age 20-45 years
- Singleton pregnancy
Who cannot join
- Known hypertensives i.e SBP>140/DBP>90/on anti-hypertensive medications prior to pregnancy
- Known diabetics (FBS>100, 75 g OGTT positive/on medications)
- Hypothyroidism
- Chronic renal failure
- Chronic liver disease
- Twin pregnancy
Show all 9Show fewer
- Known systemic inflammatory condition e.g APLA Syndrome,SLE
- Molar gestation
- Patients on nephrotoxic medications e.g.NSAIDS
Trial locations and contacts
1 site in 1 country.
India1 site, 1 recruiting
- Recruiting
All India Institute of Medical Sciences, New Delhi
New Delhi, 110029
Abhimanyu Nehra, MBBS, 9868057741, abhimanyunehra@yahoo.com
Surendra K Sharma, MD, PH.D
About this study
Hypothesis:Sleep Disorders are very common during pregnancy but the their exact role in causation of pregnancy related disorders is yet to be determined. OSA can complicate pregnancy given the risk factors of weight gain, upper displacement of the diaphragm, and hormonal-induced hyperaemia of the nasopharyngeal passages. SDB confers the risk of hypertensive disorders of pregnancy and is associated with adverse maternal and foetal outcomes.
The study would involve pregnant females which would be prospectively followed in pregnancy and post partum to know the prevalence of sleep disorders in pregnancy. Diagnosis of sleep disorders would be confirmed by overnight polysomnography and ambulatory blood pressure monitoring. Pregnancy outcomes, both maternal and fetal would be recorded and its relation with sleep disorders in pregnancy would be analysed.
Read the detailed description
Objectives
- To assess sleep quality during pregnancy
- To know prevalence of various sleep disorders during pregnancy including restless leg syndrome, symptomatic obstructive sleep apnea etc.
- To study the effect of sleep disorders on maternal and fetal outcome
- To study the relation of obstructive sleep apnea with pregnancy induced hypertension.
Material \& Methods
Study Design: Longitudinal prospective case-control study
- Consecutive patients undergoing antenatal check up at the Antenatal Clinic at AIIMS hospital during will be evaluated using questionnaires for sleep quality. Preliminary screening question for sleep disturbance in pregnancy to all patients
- Questionnaires used: Pittsburgh Sleep Quality Index (covers insomnia, RLS, snoring and sleep related breathing disorders); Epworth Sleepiness Score (for Excessive daytime sleepiness); Modified Wisconsin Score; Modified Berlin Questionnaires
- To now association between Obstructive sleep apnea and pregnancy induced hypertension patients who develop symptomatic OSA will be offered polysomnographic evaluation during the second/third trimester.
- An offer of similar services will be made to pregnant females who do not develop pregnancy induced hypertension at a similar gestational age.
Case: patient with OSA
Control: patients without OSA
- We proposed to determine that what proportion of the cases were exposed to sleep disorders and what proportion are not.
- We also planned to determine what proportion of controls is exposed and what proportion is not.
Cases and controls would be matched for age ,parity, BMI,previous h/o pre-eclampsia in first trimester.
Outcome parameters
- Prevalence of various sleep disorders in pregnancy
- Maternal outcome: Development of pregnancy induced hypertension (PIH), gestational diabetes mellitus, complicated pregnancy requiring admission, preterm delivery, ante-partum hemorrhage, delivery requiring intervention (Caesarian section, forceps/ventouse application)
- Fetal outcome: APGAR scores at 1 and 5 min, IUGR, IUD, low birth weight
Sample Size:
A sample of convenience of 200 patients (who respond to questionnaire) and satisfy inclusion and exclusion criteria will be followed up prospectively to assess the effect of sleep disorders on pregnancy outcome.As per estimates from literature sample size for case control part would be 20 for cases and 40 controls.
Investigation specifically related to projects:
- Using Somnomedic systems, GmbH polysomnography machine by trained staff nurses and technicians at:
- Obstetrics ward, AIIMS hospital
- Home based portable PSG in non admitted
- Ambulatory blood pressure by the Oscar 2™ system from SunTech Medical, USA. The Oscar 2 is clinically validated to all three internationally recognized standards.
- British Hypertension Society1 (A/A)
- European Society of Hypertension International Protocol2
- AAMI SP103 Patient comfort The Oscar 2 and the Orbit™ BP cuff make patient comfort a priority.
- The SunTech Medical, Inc. patented Orbit cuff uses an innovative stretch-sleeve design to maintain cuff placement and promote patient comfort.
- The Oscar 2 is a light, compact monitor that uses motion tolerant algorithms to reduce re-inflates and failed readings. The auto-intelligent inflation pressure also reduces measurement time, promoting patient comfort by controlling cuff inflation.
- Screening Polysomnography using Apnea linkTM PLUS
- A quick and easy sleep-screening tool designed to help identify more patients at risk for obstructive sleep apnea (OSA).
- A premium, compact device that can be used at home
Additional Investigation Required
- Routine clinical antenatal examination
- Blood pressure measurement
- Blood parameters (done routinely in ANC)
- Fasting blood sugar
- Renal and hepatic function tests
- Hemoglobin levels/s ferritin
- Serum TSH levels
- Urine examination
- Routine and spot sample for protein.
- Sonography: To rule out twin pregnancy and molar gestation/IUGR/Anomalies.
- These investigations are routinely done in ante natal clinic at AIIMS.
Data Analysis
- Data will be collected on a pre-designed proforma.
- Statistical analysis will be performed using STATA 11 for Windows software (intercooled version, Stata Corporation, Houston, TX, USA).
- After assessing for approximate normal distribution, all continuous variables will be summarized as mean ± SD or median (interquartile range).
- Categorical variables will be expressed as n (%).
- The cases and controls will be compared using unpaired t-test if the data was normally distributed and the Mann-Whitney U test if not.
- A p values of <0.05 will be considered statistically significant.
- Confounding factors influencing pregnancy outcomes will be subject to multivariate analysis to determine significance.
- Conditions
- Obstructive Sleep Apnea, Pregnancy Induced Hypertension, High-Risk Pregnancy, Restless Leg Syndrome, Infant, Very Low Birth Weight
- Being tested
- Polysomnography and ambulatory blood pressure recording
- Keywords
- Obstructive Sleep Apnea in pregnancy, Pregnancy induced hypertension, Restless leg syndrome, Sleep
- Medical subject headings
- Sleep Apnea, Obstructive, Hypertension, Pregnancy-Induced, Restless Legs Syndrome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Polysomnography and ambulatory blood pressure recordingOther
| Study group | Role | What they receive |
|---|---|---|
| polysomnography and AMBP on pregnant females | Experimental | Consecutive patients undergoing antenatal check up at the Antenatal Clinic at AIIMS hospital and obstetrics wards will be recruited and followed.Using Somnomedic systems, GmbH polysomnography machine by trained staff nurses and technicians at:
Obstetrics ward, AIIMS hospital Receives: Other: Polysomnography and ambulatory blood pressure recording |
What is being measured
The primary outcome is the main question the study is designed to answer.
Sleep quality in pregnancy and its association with pregnancy outcomes
Measured: from recruitment during pregnancy to 6 weeks post partum
Secondary outcomes (1)
Number of patients who develop PIH and gestational diabetes
Measured: from recruitment to 6 weeks post partum
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Dec 2013 (estimated)
- Study startMar 2013
- Primary completionMar 2014 (estimated)
- Study completionMay 2014 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Obstructive Sleep ApneaStudies of the same condition, open and under way.
- 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Screening
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- All India Institute of Medical Sciences
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, S.K.SHARMA, All India Institute of Medical Sciences
- Investigators
- Surendra K Sharma, MD, Ph.D., Principal investigator, All India Institute of Medical Sciences
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02016638
- Sponsor's protocol ID
- SKS/Med/Sleep_Preg
- Status last verified
- Dec 2013
- First submitted
- 2 Dec 2013
- Last updated
- 20 Dec 2013
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 20 Dec 2013. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Sleep Quality in Pregnancy and Its Impact on Pregnancy Outcomes
- ClinicalTrials.gov ID
- NCT02016638
- Acronym / sponsor ID
- SKS/Med/Sleep_Preg
- Conditions
- Obstructive Sleep Apnea, Pregnancy Induced Hypertension, High-Risk Pregnancy, Restless Leg Syndrome, Infant, Very Low Birth Weight
- Keywords
- Obstructive Sleep Apnea in pregnancy, Pregnancy induced hypertension, Restless leg syndrome, Sleep
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- All India Institute of Medical SciencesUniversity, hospital or other
- Study start
- Mar 2013
- Primary completion
- Mar 2014 (estimated)
- Study completion
- May 2014 (estimated)
- First posted
- 20 Dec 2013 (estimated)
- 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.
Hypothesis:Sleep Disorders are very common during pregnancy but the their exact role in causation of pregnancy related disorders is yet to be determined. OSA can complicate pregnancy given the risk factors of weight gain, upper displacement of the diaphragm, and hormonal-induced hyperaemia of the nasopharyngeal passages. SDB confers the risk of hypertensive disorders of pregnancy and is associated with adverse maternal and foetal outcomes.
The study would involve pregnant females which would be prospectively followed in pregnancy and post partum to know the prevalence of sleep disorders in pregnancy. Diagnosis of sleep disorders would be confirmed by overnight polysomnography and ambulatory blood pressure monitoring. Pregnancy outcomes, both maternal and fetal would be recorded and its relation with sleep disorders in pregnancy would be analysed.
Detailed description
Objectives
- To assess sleep quality during pregnancy
- To know prevalence of various sleep disorders during pregnancy including restless leg syndrome, symptomatic obstructive sleep apnea etc.
- To study the effect of sleep disorders on maternal and fetal outcome
- To study the relation of obstructive sleep apnea with pregnancy induced hypertension.
Material \& Methods
Study Design: Longitudinal prospective case-control study
- Consecutive patients undergoing antenatal check up at the Antenatal Clinic at AIIMS hospital during will be evaluated using questionnaires for sleep quality. Preliminary screening question for sleep disturbance in pregnancy to all patients
- Questionnaires used: Pittsburgh Sleep Quality Index (covers insomnia, RLS, snoring and sleep related breathing disorders); Epworth Sleepiness Score (for Excessive daytime sleepiness); Modified Wisconsin Score; Modified Berlin Questionnaires
- To now association between Obstructive sleep apnea and pregnancy induced hypertension patients who develop symptomatic OSA will be offered polysomnographic evaluation during the second/third trimester.
- An offer of similar services will be made to pregnant females who do not develop pregnancy induced hypertension at a similar gestational age.
Case: patient with OSA
Control: patients without OSA
- We proposed to determine that what proportion of the cases were exposed to sleep disorders and what proportion are not.
- We also planned to determine what proportion of controls is exposed and what proportion is not.
Cases and controls would be matched for age ,parity, BMI,previous h/o pre-eclampsia in first trimester.
Outcome parameters
- Prevalence of various sleep disorders in pregnancy
- Maternal outcome: Development of pregnancy induced hypertension (PIH), gestational diabetes mellitus, complicated pregnancy requiring admission, preterm delivery, ante-partum hemorrhage, delivery requiring intervention (Caesarian section, forceps/ventouse application)
- Fetal outcome: APGAR scores at 1 and 5 min, IUGR, IUD, low birth weight
Sample Size:
A sample of convenience of 200 patients (who respond to questionnaire) and satisfy inclusion and exclusion criteria will be followed up prospectively to assess the effect of sleep disorders on pregnancy outcome.As per estimates from literature sample size for case control part would be 20 for cases and 40 controls.
Investigation specifically related to projects:
- Using Somnomedic systems, GmbH polysomnography machine by trained staff nurses and technicians at:
- Obstetrics ward, AIIMS hospital
- Home based portable PSG in non admitted
- Ambulatory blood pressure by the Oscar 2™ system from SunTech Medical, USA. The Oscar 2 is clinically validated to all three internationally recognized standards.
- British Hypertension Society1 (A/A)
- European Society of Hypertension International Protocol2
- AAMI SP103 Patient comfort The Oscar 2 and the Orbit™ BP cuff make patient comfort a priority.
- The SunTech Medical, Inc. patented Orbit cuff uses an innovative stretch-sleeve design to maintain cuff placement and promote patient comfort.
- The Oscar 2 is a light, compact monitor that uses motion tolerant algorithms to reduce re-inflates and failed readings. The auto-intelligent inflation pressure also reduces measurement time, promoting patient comfort by controlling cuff inflation.
- Screening Polysomnography using Apnea linkTM PLUS
- A quick and easy sleep-screening tool designed to help identify more patients at risk for obstructive sleep apnea (OSA).
- A premium, compact device that can be used at home
Additional Investigation Required
- Routine clinical antenatal examination
- Blood pressure measurement
- Blood parameters (done routinely in ANC)
- Fasting blood sugar
- Renal and hepatic function tests
- Hemoglobin levels/s ferritin
- Serum TSH levels
- Urine examination
- Routine and spot sample for protein.
- Sonography: To rule out twin pregnancy and molar gestation/IUGR/Anomalies.
- These investigations are routinely done in ante natal clinic at AIIMS.
Data Analysis
- Data will be collected on a pre-designed proforma.
- Statistical analysis will be performed using STATA 11 for Windows software (intercooled version, Stata Corporation, Houston, TX, USA).
- After assessing for approximate normal distribution, all continuous variables will be summarized as mean ± SD or median (interquartile range).
- Categorical variables will be expressed as n (%).
- The cases and controls will be compared using unpaired t-test if the data was normally distributed and the Mann-Whitney U test if not.
- A p values of <0.05 will be considered statistically significant.
- Confounding factors influencing pregnancy outcomes will be subject to multivariate analysis to determine significance.
Study design
- Primary purpose
- Screening
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| polysomnography and AMBP on pregnant females | Experimental | Other: Polysomnography and ambulatory blood pressure recordingConsecutive patients undergoing antenatal check up at the Antenatal Clinic at AIIMS hospital and obstetrics wards will be recruited and followed.Using Somnomedic systems, GmbH polysomnography machine by trained staff nurses and technicians at: Obstetrics ward, AIIMS hospital |
Who may qualify
- Ages
- 20 to 45 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (2 listed)
- Age 20-45 years
- Singleton pregnancy
Key exclusion criteria (9 listed)
- Known hypertensives i.e SBP>140/DBP>90/on anti-hypertensive medications prior to pregnancy
- Known diabetics (FBS>100, 75 g OGTT positive/on medications)
- Hypothyroidism
- Chronic renal failure
- Chronic liver disease
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Polysomnography and ambulatory blood pressure recording | Other | polysomnography and AMBP on pregnant females |
Primary outcome
Sleep quality in pregnancy and its association with pregnancy outcomes
Time frame: from recruitment during pregnancy to 6 weeks post partum
1 secondary outcome
Number of patients who develop PIH and gestational diabetes
Time frame: from recruitment to 6 weeks post partum
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Dec 2013.
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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.
Surendra K Sharma, MD, Ph.D. principal investigator
All India Institute of Medical Sciences
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Polysomnography and ambulatory blood pressure recording in people with Obstructive Sleep Apnea and Pregnancy Induced Hypertension, run by All India Institute of Medical Sciences at 1 site in India.
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 2 inclusion and 9 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 20 Dec 2013. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in India. 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 Abhimanyu Nehra, MBBS (9868057741, abhimanyunehra@yahoo.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Sleep quality in pregnancy and its association with pregnancy outcomes (time frame: from recruitment during pregnancy to 6 weeks post partum). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 20 Dec 2013.