Page last updated: 2024-10-16

ammonium hydroxide and Abdominal Migraine

ammonium hydroxide has been researched along with Abdominal Migraine in 5 studies

azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.

Research Excerpts

ExcerptRelevanceReference
"Although patients diagnosed as having migraine, have been studied extensively, there is no definite proof of a primary biochemical abnormality which is of significance in the pathogenesis of migraine."1.26Further observation on the possible relationship between migraine and serum ammonia levels. ( Bruyn, GW; de Bruijn, JG; Klawans, HL, 1976)

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19904 (80.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Stankewitz, A1
Voit, HL1
Bingel, U1
Peschke, C1
May, A1
Rivas Nuñez, CJ1
Fernandez Martin, F1
de Bruijn, JG1
Bruyn, GW1
Klawans, HL1
Gilchrist, JM1
Coleman, RA1
Szám, I1
Eckhardt, S1
Németh, O1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Use of the Tx360 Nasal Applicator for Transnasal Sphenopalatine Ganglion Block in the Treatment of Chronic Migraine: A Double-blind Placebo-controlled Study[NCT01709708]Phase 441 participants (Actual)Interventional2012-09-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Acute Medications Usage

Number of acute medications used during Treatment period (6 weeks) and Follow-Up (4 weeks) (Group A vs. Group B). (NCT01709708)
Timeframe: 10 Weeks

InterventionNumber of medications used (Mean)
Marcaine29.3
Saline47.4

Adverse Events

Number of adverse events over the entire length of study (Group A vs. Group B). (NCT01709708)
Timeframe: 34 weeks

InterventionNumber of Adverse Events (Mean)
Marcaine7.67
Saline5.29

Change in Numeric Rating Scale (NRS)

Compare percentage change in Numeric Rating Scale (NRS) score from Before Procedure to 15-Minutes, Before Procedure to 30-Minutes, Before Procedure to 24-Hours After Procedure for all 12 treatments (Mean of all 12 treatments for each timepoint, comparing Group A to Group B). NRS is a likert scale ranging from 0-10 with 0 being no pain and 10 being worst possible pain. (NCT01709708)
Timeframe: 15 Minutes Post Treatment, 30 minutes Post Treatment and 24 hours Post Treatment, assessed up to 6 weeks

,
Interventionpercentage of change (Mean)
15 Minutes Post Treatment30 Minutes Post Treatment24 Hours Post Treatment
Marcaine-23.3-27.7-15.5
Saline-4.31-5.4113.5

Headache Impact Test (HIT-6)

"Total Headache Impact Test (HIT-6) scores Pre-Treatment at Visit 2 vs. Post-Treatment (following final treatment), and at 1-Month Post-Treatment (Group A vs. Group B). HIT-6 is a series of 6 likert scale questions ranging from 1 to 5 with 1 being never and 5 being always. The HIT-6 answer options are weighted as follows: Never (1) = 6 points each, Rarely (2) = 9 points each, Sometimes (3) = 10 points each, Very often (4) = 11 points each, Always (5) = 13 points each. The total score for the HIT-6 ranges from 36 (subject answers all 6 questions as Never) to 78 subject answers all 6 questions as Always), with higher total scores indicating more impact than lower scores, i.e., headaches cause greater impact on the subject's life." (NCT01709708)
Timeframe: 10 Weeks

,
Interventionunits on a scale (Mean)
Pre-TreatmentPost-Treatment1-Month Post-Treatment
Marcaine64.3659.8559.23
Saline6462.561.92

Migraine Headache Days

Compare change in the number of migraine headache days per month reported in Baseline Period Diary vs. Treatment Period Diary vs. Post-Treatment Period Diary. (NCT01709708)
Timeframe: 12 Weeks

,
InterventionMigraine headache days per month (Mean)
BaselineTreatmentPost Treatment
Marcaine15.012.310.8
Saline15.812.211.3

Modified Pain Characteristic Questionnaire

Compare Modified Pain Characteristic Questionnaire scores Before Procedure vs. 24-Hour After Procedure, Before Procedure vs. 1-Month Follow Up, and Before Procedure vs. 6-Month Follow Up (Mean of all 12 treatments for each timepoint, comparing Group A to Group B). The modified pain characteristic questionnaire is a series of 11 questions on a likert scale ranging from 0 to 10 with 0 being no pain or does not interfere and 10 being worst pain or completely interferes. Percentage questions range from 0 to 100. (NCT01709708)
Timeframe: Before Treatment, 24 Hours After Treatment, 1 Month Post Treatment, and 6 Months Post Treatment

,
Interventionunits on a scale (Mean)
Worst Pain Question: Before TreatmentWorst Pain Question: 24 Hours After TreatmentWorst Pain Question: 1 Month Post TreatmentWorst Pain Question: 6 Months Post TreatmentLeast Pain Question: Before TreatmentLeast Pain Question: 24 Hours After TreatmentLeast Pain Question: 1 Month Post TreatmentLeast Pain Question: 6 Months Post TreatmentAverage Pain Question: Before TreatmentAverage Pain Question: 24 Hours After TreatmentAverage Pain Question: 1 Month Post TreatmentAverage Pain Question: 6 Months Post TreatmentPercent Relief Question: Before TreatmentPercent Relief Question: 24 Hours After TreatmentPercent Relief Question: 1 Month Post TreatmentPercent Relief Question: 6 Months Post TreatmentGeneral Activity Question: Before TreatmentGeneral Activity Question: 24 Hours After TreatmenGeneral Activity Question: 1 Month Post TreatmentGeneral Activity Question: 6 Months Post TreatmentMood Interference Question: Before TreatmentMood Interference Question: 24 Hours After TreatmeMood Interference Question: 1 Month Post TreatmentMood Interference Question: 6 Months Post TreatmenWalking Ability Question: Before TreatmentWalking Ability Question: 24 Hours After TreatmentWalking Ability Question: 1 Month Post TreatmentWalking Ability Question: 6 Months Post TreatmentNormal Work Question: Before TreatmentNormal Work Question: 24 Hours After TreatmentNormal Work Question: 1 Month Post TreatmentNormal Work Question: 6 Months Post TreatmentRelationships Question: Before TreatmentRelationships Question: 24 Hours After TreatmentRelationships Question: 1 Month Post TreatmentRelationships Question: 6 Months Post TreatmentSleep Interference Question: Before TreatmentSleep Interfere Question: 24 Hours After TreatmentSleep Interferenc Question: 1 Month Post TreatmentSleep Interference Question: 6 Months Post TreatmeEnjoyment Question: Before TreatmentEnjoyment Question: 24 Hours After TreatmentEnjoyment Question: 1 Month Post TreatmentEnjoyment Question: 6 Months Post Treatment
Marcaine4.754.364.564.272.011.771.881.683.393.073.362.8641.346.046.334.72.492.312.642.682.572.422.963.180.630.540.800.452.532.212.522.592.001.962.362.052.291.891.921.552.812.582.643.18
Saline6.156.165.645.882.502.432.642.884.334.273.914.0029.229.821.018.63.503.643.914.003.784.193.825.711.271.240.550.433.493.633.453.713.473.903.093.862.682.852.553.143.123.343.094.00

Numeric Rating Scale (NRS)

Compare Numeric Rating Scale (NRS) scores Before Procedure,15-Minute Post Treatment, 30-Minutes Post Treatment, 24-Hour Post Treatment for all 12 treatments (Marcaine vs. Saline). NRS is a likert scale ranging from 0-10 with 0 being no pain and 10 being worst possible pain. For each individual time point, all 12 treatments were averaged for that time point and a single value was used for comparison between the two groups. (NCT01709708)
Timeframe: 6 Weeks

,
Interventionunits on a scale (Mean)
Before Procedure15 Minutes Post Treatment30 Minutes Post Treatment24 Hours Post Treatment
Marcaine3.182.532.412.85
Saline3.783.513.454.20

Overall Satisfaction

Satisfaction scores Visit 2 vs. following treatment (Treatment 12) and at 1-Month Post-Treatment (Group A vs. Group B). Satisfaction scores are a likert scale ranging from 1 to 5 with 1 being complete dissatisfaction and 5 being complete satisfaction. (NCT01709708)
Timeframe: 10 Weeks

,
Interventionunits on a scale (Mean)
Visit 2Following treatment (Treatment 12)1-Month Post-Treatment
Marcaine3.523.553.57
Saline3.002.502.64

Patient's Global Impression of Change (PGIC)

Compare 24-Hour After Procedure Patient's Global Impression of Change (PGIC) score for 12 treatments (Mean of all 12 treatments for each timepoint, comparing Group A to Group B). PGIC is a likert scale ranging from 1 to 7 with 1 being very much improved and 7 being very much worse. (NCT01709708)
Timeframe: 30 minutes Post Treatment and 24 hours Post Treatment, assessed up to 6 weeks

,
Interventionunits on a scale (Mean)
30 Minutes Post Treatment24 Hours Post Treatment
Marcaine3.003.08
Saline3.723.88

Reviews

1 review available for ammonium hydroxide and Abdominal Migraine

ArticleYear
[Biochemical aspects of migraine].
    Revista clinica espanola, 1975, Oct-31, Volume: 139, Issue:2

    Topics: 5-Hydroxytryptophan; Age Factors; Ammonia; Blood Platelet Disorders; Female; Humans; Menstruation; M

1975

Other Studies

4 other studies available for ammonium hydroxide and Abdominal Migraine

ArticleYear
A new trigemino-nociceptive stimulation model for event-related fMRI.
    Cephalalgia : an international journal of headache, 2010, Volume: 30, Issue:4

    Topics: Adult; Ammonia; Brain Stem; Female; Humans; Irritants; Magnetic Resonance Imaging; Male; Migraine Di

2010
Further observation on the possible relationship between migraine and serum ammonia levels.
    Clinical neurology and neurosurgery, 1976, Volume: 79, Issue:2

    Topics: Adult; Ammonia; Humans; Migraine Disorders

1976
Ornithine transcarbamylase deficiency: adult onset of severe symptoms.
    Annals of internal medicine, 1987, Volume: 106, Issue:4

    Topics: Adult; Ammonia; Brain Diseases, Metabolic; Female; Hemiplegia; Heterozygote; Humans; Mental Disorder

1987
[Further studies on clopamide].
    Medizinische Monatsschrift, 1970, Volume: 24, Issue:8

    Topics: Adult; Amides; Ammonia; Clopamide; Diuretics; Female; Humans; Hypertension; Lymphedema; Male; Middle

1970