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Anxiety and Recurrent Abdominal Pain in Children

Primary Purpose

Abdominal Pain, Anxiety

Status

Completed

Phase

Phase 2

Locations

United States

Study Type

Interventional

Intervention

Citalopram

Placebo

About this trial

This is an interventional treatment trial for Abdominal Pain focused on measuring Abdominal Pain, Anxiety

Eligibility Criteria

7 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

At least 3 episodes of abdominal pain during the previous 3 months associated with functional impairment in the absence of explanatory physical disease following clinically appropriate medical assessment.
Age 7 years 0 months to 18 years 11 months, inclusive, at initial evaluation.
Significant global functional impairment as reflected by a score less than 70 on the Children's Global Assessment Scale
Residing with a primary caretaker (i.e., parent, legal guardian, relative functioning as a parent, or foster parent) who has known the child well for at least 6 months prior to study entry and has legal authority to consent to participation.

Exclusion Criteria:

Physical disease sufficient to explain the subjective distress and functional impairment suffered by the subject.
FAP with atypical features:
1. Abnormal abdominal or rectal examination
2. GI bleeding (i.e., hematest positive stool or hematemesis)
3. History of recurrent or persistent fever associated with the abdominal pain
4. Involuntary weight loss (> 5% of body weight) over the previous 3 months
5. Previous laboratory evidence suggesting explanatory physical disease
6. Persistent nighttime awakenings due to abdominal pain (at least once per week and > 4 per month)
7. Persistent or bilious vomiting (at least once per week and > 4 per month)
8. Abdominal pain exclusively associated with menstruation
9. Dysuria
Physical disease in which citalopram monotherapy or study participation might prove to be disadvantageous or incompatible with quality care, including bleeding disorder characterized by prolonged bleeding time, uncontrolled epilepsy, or poorly controlled diabetes mellitus.
Psychiatric problem or disorder in which citalopram monotherapy or study participation might prove to be disadvantageous or incompatible with quality care, including evidence that the child is a serious acute danger to self or others, anorexia nervosa, bulimia nervosa, schizophrenia, schizoaffective disorder, alcohol or substance abuse/dependence, or bipolar disorder.
History of mental retardation as defined by full scale IQ < 70 on previous testing or participation in special education placement for mild to severe mental retardation.
Inadequate English speaking abilities of child or parent(s) to complete study measures and/or communicate with study examiners.
Adequate prior trial of citalopram, escitalopram, or another selective serotonin reuptake inhibitor or venlafaxine. Adequate trial is defined as at least 4 weeks of citalopram 20 mg/day, escitalopram 10 mg/day, fluoxetine 20 mg/day, fluvoxamine 100 mg/day, paroxetine 20 mg/day, sertraline 50 mg/day, or venlafaxine 75 mg/day.
Concurrent use of non-steroidal anti-inflammatory drugs (NSAIDs), aspirin, or anticoagulant medications.
Treatment for physical or psychiatric illness initiated within the prior 4 weeks or escalating in dosage or intensity.
History of hypersensitivity to citalopram or serotonin-syndrome.
Participation in any investigational drug study within thirty days of study entry.
Pregnancy
Sexually active female subjects refusing to use a medically accepted method of birth control during the study, or who engaged in unprotected sexual activity during the 30 days prior to the study.

Sites / Locations

The Research Institute at Nationwide Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Citalopram

Placebo

Arm Description

Citalopram was initiated at 10 mg daily for one week, with dosage increased to 20 mg daily during week 2, with an optional increase to 40 mg daily at week 4 or thereafter if response was judged to be suboptimal (CGI-I or CGI-S > 2).

Placebo administered in capsules identical to those containing citalopram using microcrystalline cellulose.

Outcomes

Primary Outcome Measures

Clinical Global Impression Scale - Improvement (CGI-I) Will be Used to Assess Overall Global Illness Improvement. CGI-I Scores of 1 (Very Much Improved) or 2 (Much Improved) Indicate an Acceptable Treatment Response.

Clinical Global Impression Scale - Improvement (CGI-I) is a 7-point scale, with lower values being more favorable, used to assess overall global illness improvement. The CGI is a clinician-completed measure, with values ranging from 1 (very much improved), 2 (much improved), 3 (minimally improved), 4 (no change), 5 (minimally worse), 6 (much worse), to 7 (very much worse). CGI-I scores of 1 (very much improved) or 2 (much improved) were considered to indicate an acceptable treatment response. A global measure of functional status was chosen as a primary outcome due to the broad array of symptomatology seen in pediatric RAP and the ambiguous relationship between functional status and symptoms of pain, anxiety, and depression in pediatric RAP. The CGI-I is a dichotomous primary outcome measure of global clinical improvement with clinical response be defined as a CGI-I score of 1 or 2 for at least two consecutive weeks.

Clinical Global Impression Scale - Severity (CGI-S)

Clinical Global Impression Scale - Severity (CGI-S) is a 7-point scale is a clinician-completed measure that requires the clinician to rate the severity of the patient's illness at the time of assessment relative to the clinician's past experience with patients who have the same diagnosis. Considering total clinical experience, a patient is assessed on severity of illness at the time of rating, with values ranging from 1 (normal, not at all ill), 2 (borderline ill), 3 (mildly ill), 4 (moderately ill), 5 (markedly ill), 6 (severely ill), to 7 (extremely ill).

Abdominal Pain Index (API)

The API is a well-validated and reliable measure of abdominal pain assessing the frequency, duration, and intensity of abdominal pain consisting of five items assessing the frequency, duration, and intensity of abdominal pain experienced during the prior 2 weeks. Two of the items are scored from 0 to 5, one is scaled 0 to 8, and two are scaled 0 to 10, with lower scores considered to be better than higher scores. Item scores are standardized using Z-scores and then summed to yield an index of abdominal pain that has been sensitive to change in previous epidemiological and treatment studies of FAP. Alpha reliability ranged from 0.80 to 0.93. The API will be a continuous primary outcome measure of abdominal pain.

Secondary Outcome Measures

Pediatric Anxiety Rating Scale (PARS)

Pediatric Anxiety Rating Scale (PARS) is a clinician administered measure of anxiety in children and adolescents. The PARS is comprised of a 50-item symptom checklist used to determine the presence or absence of specific anxiety symptoms during the prior week and 7 severity/impairment items, each scored from 0 to 5 . The the score on the 7 items allows the clinician to rate symptom severity and associated impairment on a range from 0 to 35, with higher scores reflecting greater symptom severity and associated impairment. The PARS is characterized by high interrater reliability (ICC = 0.97), adequate internal consistency (α = 0.64), and fair test-retest reliability (ICC = 0.55). There is preliminary support for convergent and divergent validity, and the PARS has demonstrated sensitivity to treatment effects in previously conducted clinical trials.

Children's Depression Rating Scale - Revised (CDRS-R)

Children's Depression Rating Scale - Revised (CDRS-R) is a clinician administered measure of depression in children and adolescents and provides data necessary to diagnose depressive disorder and rate the severity of depressive symptoms over time. The CDRS-R is composed of 17 items, most rated on a 1 to 7 scale, with a minimum score of 17 and a maximum of 113. Higher scores reflect greater depression severity, with scores of 40 and above generally considered to be reflective of a depressive diagnosis.

Children's Global Assessment Scale (C-GAS)

Children's Global Assessment Scale (C-GAS) is an interview-based adaptation of the Global Assessment Scale developed to assess child and adolescent functioning during a specified time period. Scores range from one to 100, with scores of 70 or below reflecting abnormally low functioning and higher scores reflecting better functioning. The C-GAS has demonstrated reliability, as well as discriminant and concurrent validity. A CGAS score of < 70 will be a requirement at study entry.

Full Information

NCT ID

NCT00962039

First Posted

August 18, 2009

Last Updated

May 28, 2020

Sponsor

John V. Campo, M.D.

Collaborators

National Institute of Mental Health (NIMH)

1. Study Identification

Unique Protocol Identification Number

NCT00962039

Brief Title

Anxiety and Recurrent Abdominal Pain in Children

Official Title

Anxiety and Recurrent Abdominal Pain in Children

Study Type

Interventional

2. Study Status

Record Verification Date

May 2020

Overall Recruitment Status

Completed

Study Start Date

July 2004 (undefined)

Primary Completion Date

April 2010 (Actual)

Study Completion Date

April 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor-Investigator

Name of the Sponsor

John V. Campo, M.D.

Collaborators

National Institute of Mental Health (NIMH)

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Yes

Studies a U.S. FDA-regulated Device Product

Data Monitoring Committee

Yes

5. Study Description

Brief Summary

This study aims to determine whether citalopram is a useful, well-tolerated, and safe treatment for children and adolescents ages 7 to 18 years with functional abdominal pain. The study hypothesis is that citalopram will be better than placebo in producing clinical improvement and reductions in abdominal pain. It is also hypothesized that citalopram and placebo will not differ in terms of safety and tolerability.

Detailed Description

This study aims to determine the relative efficacy, tolerability, and safety of the citalopram in the treatment of pediatric functional recurrent abdominal pain (FAP) in children and adolescents ages 7 to 18 years, inclusive. The goal is to recruit and randomize 100 subjects to citalopram or placebo. Secondary aims include to determine if citalopram is superior to placebo in reducing comorbid anxiety and depressive symptoms in children and adolescents with FAP, to explore potential mediators (i.e., anxiety, depression) and moderators (e.g., age, gender, referral from primary or specialty care) of treatment response, and to explore the durability and tolerability of citalopram treatment 18 weeks following completion of the double-blind treatment phase with the goal of generating data useful to the development of future studies. The study is novel in conducting recruitment, assessment, and treatment in traditional medical settings. Limited exclusion criteria and the delivery of study assessments and interventions within routine practice settings provide for considerably greater external validity than the typical efficacy study. Study hypotheses: Citalopram will be superior to placebo in producing clinical improvement and reductions in abdominal pain. Citalopram and placebo will not differ in tolerability or safety.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Abdominal Pain, Anxiety

Keywords

Abdominal Pain, Anxiety

7. Study Design

Primary Purpose

Treatment

Study Phase

Phase 2, Phase 3

Interventional Study Model

Parallel Assignment

Masking

ParticipantCare ProviderInvestigatorOutcomes Assessor

Allocation

Randomized

Enrollment

81 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Citalopram

Arm Type

Experimental

Arm Description

Arm Title

Placebo

Arm Type

Placebo Comparator

Arm Description

Placebo administered in capsules identical to those containing citalopram using microcrystalline cellulose.

Intervention Type

Drug

Intervention Name(s)

Citalopram

Other Intervention Name(s)

Celexa

Intervention Description

Participants will be randomly assigned to citalopram or placebo in a parallel groups design for 8 weeks of double-blind treatment beginning with 10 mg per day week 1, 20 mg per day week 2, and 40 mg per day week 4 or thereafter if response is suboptimal and there are no significant side effects.

Intervention Type

Drug

Intervention Name(s)

Placebo

Intervention Description

Primary Outcome Measure Information:

Title

Description

Time Frame

The CGI will be completed at weeks 2, 4, and 8

Title

Clinical Global Impression Scale - Severity (CGI-S)

Description

Time Frame

Weeks 0, 2, 4, and 8

Title

Abdominal Pain Index (API)

Description

Time Frame

Weeks 0, 2, 4, and 8

Secondary Outcome Measure Information:

Title

Pediatric Anxiety Rating Scale (PARS)

Description

Time Frame

Weeks 0, 2, 4, and 8

Title

Children's Depression Rating Scale - Revised (CDRS-R)

Description

Time Frame

Weeks 0, 2, 4, and 8

Title

Children's Global Assessment Scale (C-GAS)

Description

Time Frame

Weeks 0, 2, 4, and 8

10. Eligibility

Sex

All

Minimum Age & Unit of Time

7 Years

Maximum Age & Unit of Time

18 Years

Accepts Healthy Volunteers

Eligibility Criteria

Inclusion Criteria: At least 3 episodes of abdominal pain during the previous 3 months associated with functional impairment in the absence of explanatory physical disease following clinically appropriate medical assessment. Age 7 years 0 months to 18 years 11 months, inclusive, at initial evaluation. Significant global functional impairment as reflected by a score less than 70 on the Children's Global Assessment Scale Residing with a primary caretaker (i.e., parent, legal guardian, relative functioning as a parent, or foster parent) who has known the child well for at least 6 months prior to study entry and has legal authority to consent to participation. Exclusion Criteria: Physical disease sufficient to explain the subjective distress and functional impairment suffered by the subject. FAP with atypical features: Abnormal abdominal or rectal examination GI bleeding (i.e., hematest positive stool or hematemesis) History of recurrent or persistent fever associated with the abdominal pain Involuntary weight loss (> 5% of body weight) over the previous 3 months Previous laboratory evidence suggesting explanatory physical disease Persistent nighttime awakenings due to abdominal pain (at least once per week and > 4 per month) Persistent or bilious vomiting (at least once per week and > 4 per month) Abdominal pain exclusively associated with menstruation Dysuria Physical disease in which citalopram monotherapy or study participation might prove to be disadvantageous or incompatible with quality care, including bleeding disorder characterized by prolonged bleeding time, uncontrolled epilepsy, or poorly controlled diabetes mellitus. Psychiatric problem or disorder in which citalopram monotherapy or study participation might prove to be disadvantageous or incompatible with quality care, including evidence that the child is a serious acute danger to self or others, anorexia nervosa, bulimia nervosa, schizophrenia, schizoaffective disorder, alcohol or substance abuse/dependence, or bipolar disorder. History of mental retardation as defined by full scale IQ < 70 on previous testing or participation in special education placement for mild to severe mental retardation. Inadequate English speaking abilities of child or parent(s) to complete study measures and/or communicate with study examiners. Adequate prior trial of citalopram, escitalopram, or another selective serotonin reuptake inhibitor or venlafaxine. Adequate trial is defined as at least 4 weeks of citalopram 20 mg/day, escitalopram 10 mg/day, fluoxetine 20 mg/day, fluvoxamine 100 mg/day, paroxetine 20 mg/day, sertraline 50 mg/day, or venlafaxine 75 mg/day. Concurrent use of non-steroidal anti-inflammatory drugs (NSAIDs), aspirin, or anticoagulant medications. Treatment for physical or psychiatric illness initiated within the prior 4 weeks or escalating in dosage or intensity. History of hypersensitivity to citalopram or serotonin-syndrome. Participation in any investigational drug study within thirty days of study entry. Pregnancy Sexually active female subjects refusing to use a medically accepted method of birth control during the study, or who engaged in unprotected sexual activity during the 30 days prior to the study.

Overall Study Officials:

First Name & Middle Initial & Last Name & Degree

John V Campo, MD

Organizational Affiliation

The Research Institute at Nationwide Children's Hospital

Official's Role

Principal Investigator

Facility Information:

Facility Name

The Research Institute at Nationwide Children's Hospital

City

Columbus

State/Province

Ohio

ZIP/Postal Code

43205

Country

United States

12. IPD Sharing Statement

Plan to Share IPD

Citations:

PubMed Identifier

15381890

Citation

Campo JV, Perel J, Lucas A, Bridge J, Ehmann M, Kalas C, Monk K, Axelson D, Birmaher B, Ryan N, Di Lorenzo C, Brent DA. Citalopram treatment of pediatric recurrent abdominal pain and comorbid internalizing disorders: an exploratory study. J Am Acad Child Adolesc Psychiatry. 2004 Oct;43(10):1234-42. doi: 10.1097/01.chi.0000136563.31709.b0.

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Anxiety and Recurrent Abdominal Pain in Children

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