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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02710825
Other study ID # 2015-A01332-47
Secondary ID
Status Completed
Phase N/A
First received March 2, 2016
Last updated February 23, 2017
Start date May 2016
Est. completion date February 23, 2017

Study information

Verified date February 2017
Source Hôpital Necker-Enfants Malades
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Osteopathic care impact on postoperative pain assessed by osteopathic session, evaluated by EVENDOL scale surgery on children with congenital heart disease


Description:

The management of pain in children after cardiac surgery is the key to ensure a better comfort and fast home return.

Aside drugs and psychology or physical therapy, no other alternative is proposed in the medico-surgical unit of pediatric cardiology at the Necker hospital.

Following a feasibility study within the department, osteopathic care showed significant pain reduction in postoperative surgery assessed through the EVENDOL scale.

The goal was mainly to improve mobility restricted areas due to the operation, and so help to reduce post-operative pain.

Investigators propose to continue the assessment of the overall osteopathic taking care of the child after heart surgery while retaining EVENDOL scale as primary endpoint. Population will include children from the age of 5 days to less than 7 years old.


Recruitment information / eligibility

Status Completed
Enrollment 113
Est. completion date February 23, 2017
Est. primary completion date February 23, 2017
Accepts healthy volunteers No
Gender All
Age group N/A to 7 Years
Eligibility Inclusion Criteria:

- Children aged 5 days to 7 years old

- Congenital heart sternotomy or thoracotomy operated

- Postoperative management at the Necker hospital in Paris, followed by Professor Damien Bonnet team

- Agreeing to participate of one of the holders of parental authority

- Oral Agreement child age

- Minimal knowledge of French language by parents

- Covered by the French social security system

Exclusion Criteria:

- Heart disease treated by interventional catheterization

- Postoperative complications requiring more than three weeks of intensive care

- Participation in an other biomedical research protocol

- Refusal or linguistic or mental disabilities or parents of the child

Study Design


Intervention

Other:
Osteopathy
The treatment begins, if possible, on the body part of the child whose osteopathic score is the highest , with the least elasticity and mobility. Then the other restricted joints will be treated. The set of techniques will be carried out after palpation and appropriate tensioning. The various actions will be carried out on the tissues and joints who have been particularly affected by the operation. When a joint or tissue has a restricted mobility in a direction or a specific movement, it will require appropriate and gently manual correction, in order to reduce and improve its functionality.
superficial palpatory agreement
The simulated treatment also begins with the body part of the child whose osteopathic score is the highest. Then the other restricted joints will be treated. The set of techniques will be carried out with the same investments as the tests , with a superficial palpatory agreement and without tensioning so that the restricted articulation or tissue will not be corrected

Locations

Country Name City State
France Hospital Necker Paris

Sponsors (2)

Lead Sponsor Collaborator
Hôpital Necker-Enfants Malades ARCFA : Association for research in cardiology foetal to adult

Country where clinical trial is conducted

France, 

References & Publications (2)

Degenhardt BF, Kuchera ML. Osteopathic evaluation and manipulative treatment in reducing the morbidity of otitis media: a pilot study. J Am Osteopath Assoc. 2006 Jun;106(6):327-34. — View Citation

Guiney PA, Chou R, Vianna A, Lovenheim J. Effects of osteopathic manipulative treatment on pediatric patients with asthma: a randomized controlled trial. J Am Osteopath Assoc. 2005 Jan;105(1):7-12. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change of EVENDOL from day1 at day2 Pain Rating Scale and discomfort in children, giving a score from 0 to 15 filled by doctor day 2
Secondary Change of EVENDOL from day1 at day2 Pain Rating Scale and discomfort in children, giving a score from 0 to 15 filled by children's parent (mother or father) day 2
Secondary Change of Score OSCAR from day1 at day2 OS : for osteopathy CAR : for cardiopathy Osteopathic Scale assessing the mobility of each part of the body to give a final score OSCAR ranging from 0 to 45. day 2
Secondary Change of Faces scale or Visual analog scale from day1 at day2 Pain Rating Scale and discomfort in children giving a score from 0 to 10 filled by child day 2
Secondary Change of Arterial Pressure from day1 at day2 Day 2
Secondary Change of Oxygen saturation from day1 at day2 day2
Secondary Change of cardiac frequency from day1 at day2 day 2
Secondary Change of cardiac breathing frequency from day1 at day2 day2
Secondary Analgesic intake at day1 Doctor's drugs prescription day1
Secondary Analgesic intake at day2 Doctor's drugs prescription day2
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